IP Library › Granted Patent US 10,669,298
Granted Patent B2
US 10,669,298 · App. 15/945,221 · Granted Jun 2, 2020

Mannose derivatives for treating bacterial infections

Inventors: Yeeman K. Ramtohul (Pierrefonds, CA); Sanjoy Kumar Das (Pierrefonds, CA); Caroline Cadilhac (Montreal, CA); Thumkunta Jagadeeswar Reddy (Pierrefonds, CA); Louis Vaillancourt (Laval, CA); Michel Gallant (Pierrefonds, CA); Bingcan Liu (Montreal, CA); Evelyne Dietrich (Laval, CA); Frederic Vallee (Montreal, CA); Julien Martel (Montreal, CA); Carl Poisson (Montreal, CA)
Assignee: Vertex Pharmaceuticals Incorporated
C07H7/02A61K31/706A61K31/7028A61K31/7034A61K31/7036A61K31/7042A61K31/7048A61K31/7056A61K31/7064C07D309/10C07D405/14C07D407/14C07D409/14C07D413/14C07D417/14C07D495/04C07H7/04C07H7/06C07H15/26C07H19/02C07H19/056Y02A50/473
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,669,298
App. No.
15/945,221
Granted
Jun 2, 2020
Kind
B2
Abstract

The present invention relates to compounds useful for the treatment or prevention of bacteria infections. These compounds have formula I: The invention also provides pharmaceutically acceptable compositions containing the compounds and methods of using the compositions in the treatment of bacteria infections. Finally, the invention provides processes for making compounds of the invention.

Claims (194)

1. A compound of Formula I, or a pharmaceutically acceptable salt thereof:

wherein

Z is

Ring H is an optionally substituted 5-6 membered aromatic monocyclic ring optionally having 1-4 heteroatoms selected from nitrogen, or sulfur; an 8-12 membered aromatic bicyclic ring optionally having 1-6 heteroatoms selected from oxygen, nitrogen, or sulfur; or a 10-14 membered aromatic tricyclic ring optionally having 1-6 heteroatoms selected from oxygen, nitrogen, or sulfur;

L 2 is —X 2 Y 2 —wherein X 2 is a C 1 aliphatic or —C(O)— and Y 2 is C 1 -C 10 aliphatic wherein up to two methylene units of the C 1 -C 10 aliphatic are optionally replaced with —C(O)—, NH, or N(C 1 -C 6 aliphatic); L 2 is optionally substituted with 1-3 halo;

L 3 is C 1 -C 12 aliphatic wherein up to three methylene units of the C 1 -C 12 aliphatic are optionally replaced with —C(O)—, NH, or N(C 1 -C 6 aliphatic); L 3 is optionally substituted with 1-3 halo;

each J H is independently halogen, —CN, —NO 2 , X J , Q J , or X J -Q J ; or two J H groups bound to the same carbon atom, together with the carbon atom to which they are bound, optionally form —C═N—OH, —C(O)—, or Ring HH;

Ring HH is a 3-8 membered saturated monocyclic ring having 0-2 heteroatoms selected from oxygen, nitrogen, or sulfur; optionally substituted with 1-4 occurrences of J HH ;

J HH is halo, CN, oxo, X J , Q J , or X J -Q J ;

X J is a C 1 -C 10 aliphatic, wherein up to 4 methylene units of the C 1 -C 10 aliphatic are optionally replaced with —O—, —NH, N(C 1 C 6 aliphatic), —S—, —C(O)—, —C(═NOH)—,—S(O)—, —S(O) 2 —, P, or P(O); X J is optionally substituted with 0-6 occurrences of halo, OH, or C 1-4 alkyl; or optionally substituted with 0-1 occurrences of CN and;

Q J is a 3-7 membered monocyclic saturated, fully unsaturated, partially unsaturated, or aromatic ring optionally having 1-4 heteroatoms selected from oxygen, nitrogen, or sulfur; or an 8-12 membered saturated, fully unsaturated, partially unsaturated, or aromatic ring optionally having 1-6 heteroatoms selected from oxygen, nitrogen, or sulfur; wherein each Q J is optionally substituted with 1-6 occurrences of halo, oxo, CN, or C 1-6 alkyl, wherein up to 2 methylene units of said C 1-6 alkyl are optionally replaced with —O—, —NH, N(C 1 -C 6 aliphatic), —S—, —C(O)—, —S(O)—, or —S(O) 2 —.

2. The compound of claim 1 , wherein Ring H, is phenyl, napthyl, or a 5-6 membered heteroaryl having 1-4 heteroatoms selected from oxygen, nitrogen, or sulfur.

3. The compound of claim 1 , wherein Z is

and

J H is halo, CN, NO 2 , phenyl, or C 1-10 aliphatic wherein up to 3 methylene units are optionally replaced with O, NH, N(C 1-4 alkyl), S, C(O), SO, or SO 2 ; wherein said J H is optionally substituted with 1-3 occurrences of CN, halo or phenyl.

4. The compound of claim 3 wherein

L 2 is C 1-6 aliphatic or (C 1-4 aliphatic)-C(O)NH—;

L 3 is C 1-6 aliphatic or —NHC(O)—(C 1-4 aliphatic)-;

Ring H is phenyl or naphthyl; and

J H is halo, CN, NO 2 , C 1-6 aliphatic, —OC 1-6 aliphatic, or C(O)O(C 1-6 aliphatic); wherein

said J H is optionally substituted with 1-3 occurrences of halo.

5. The compound of claim 1 , wherein L 2 and L 3 are each independently C 1 -C 4 alkenyl or C 1 -C 4 alkynyl.

6. The compound of claim 1 , having formula IB:

7. The compound of claim 6 , wherein L 2 and L 3 are bonded to the mannose ring via a carbon atom.

8. The compound of claim 7 , wherein L 2 and L 3 are each independently C 1 -C 6 alkenyl or C 1 -C 6 alkynyl.

9. The compound of claim 8 , wherein at least one of L 2 and L 3 is —C≡C—.

10. The compound of claim 1 , having formula ID:

11. The compound of claim 10 , wherein Ring H is an optionally substituted 5-6 membered monocyclic aromatic ring optionally having 1-4 heteroatoms selected from nitrogen, or sulfur; or an 8-12 membered bicyclic aromatic ring optionally having 1-6 heteroatoms selected from oxygen, nitrogen, or sulfur; or a 10-14 tricyclic aromatic ring optionally having 1-6 heteroatoms selected from oxygen, nitrogen, or sulfur.

12. The compound of claim 11 , wherein Ring H is optionally substituted phenyl, naphthyl, thienyl, isoxazolyl, pyridinyl, pyrazinyl, indolyl, indazolyl, thienylthiophenyl, quinolinyl, quinazolinyl, benzothiadiazolyl, or fluorenyl.

13. The compound of claim 10 , wherein Ring H, together with J H and J HH , is selected from the following:

14. The compound of claim 10 , wherein J H is halogen, oxo, CN,

Q J , or X J -Q J ; wherein

X J is C 1 -C 10 aliphatic, wherein up to 4 methylene units of the C 1 -C 10 aliphatic are optionally replaced with —O—, —NH, N(C 1 -C 6 aliphatic), —S—, —C(O)—, —S(O)—, —S(O) 2 —;

Q J is phenyl; and

J H is optionally substituted with 0-3 occurrences of halo or 0-1 occurrences of CN.

15. The compound of claim 14 , wherein J H is halogen, CN, —C(CH 3 ) 2 CN, C 3-6 cycloalkyl, phenyl, —O—CH 2 phenyl, or C 1-6 alkyl wherein up to one methylene unit is optionally replaced with —O—, —S—, —NH—, —N(C 1-6 alkyl)-, or —C(O)—; wherein said J H is substituted with 0-3 halo or 0-1 CN.

16. The compound of claim 10 , wherein Ring H is optionally substituted phenyl or naphthyl.

17. The compound of claim 16 , wherein Ring H is phenyl and J H is halo, CN, —C(CH 3 ) 2 CN, C 3-6 cycloalkyl, phenyl, CH 2 phenyl, —O—CH 2 phenyl, or C 1-6 alkyl wherein up to one methylene unit is optionally replaced with —O—, —S—, —NH—, —N(C 1-6 alkyl)-, or —C(O)—; wherein said J H is substituted with 0-3 halo or 0-1 CN.

18. The compound of claim 1 , represented by a structural formula selected from the group consisting of:

#

Structure

 69

 70

 71

 72

 73

 74

 75

 76

 77

 78

 79

 80

 81

 82

 83

 84

 85

 86

 87

 88

 89

 90

 91

 92

 93

 94

 95

 96

 97

 98

 99

100

101

102

103

104

105

106

107

108

109

110

111

112

113

114

115

116

117

118

119

120

123

125

126

128

130

131

132

133

134

135

136

137

138

158

161

162

163

164

165

166

167

168

169

170

171

173

174

175

176

177

178

179

180

181

182

183

184

185

186

187

188

189

190

191

192

193

194

195

196

197

198

199

200

201

202

203

204

205

206

207

208

209

210

211

212

213

214

215

216

217

218

219

220

221

222

223

224

225

226

227

228

229

230

231

232

233

234

235

236

237

238

239

240

241

242

243

244

245

or a pharmaceutically acceptable salt thereof.

19. The compound of claim 18 , wherein the compound is compound 53:

20. A composition comprising the compound of claim 1 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, adjuvant, or vehicle.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 8, 2019
From: RAMTOHUL, YEEMAN K.; DAS, SANJOY KUMAR; CADILHAC, CAROLINE; REDDY, THUMKUNTA JAGADEESWAR; VAILLANCOURT, LOUIS; GALLANT, MICHEL; LIU, BINGCAN; DIETRICH, EVELYNE; VALLEE, FREDERIC; MARTEL, JULIEN; POISSON, CARL
To: VERTEX PHARMACEUTICALS (CANADA) INCORPORATED
Reel/Frame 047927/0299 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 8, 2019
From: VERTEX PHARMACEUTICALS (CANADA) INCORPORATED
To: VERTEX PHARMACEUTICALS INCORPORATED
Reel/Frame 047927/0472 →
Continuity (6)
Continuation 15140045 · Apr 27, 2016
Division 14132662 · Dec 18, 2013
Provisional Application 61874501 · Sep 6, 2013
Provisional Application 61788241 · Mar 15, 2013
Provisional Application 61738620 · Dec 18, 2012
Related Publication 20190106450A1 · Apr 11, 2019