IP Library Granted Patent US 7,186,828
Granted Patent B2
US 7,186,828 · App. 10/311,178 · Granted Mar 6, 2007

Cyclic urea compounds and preparation thereof

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 7,186,828
App. No.
10/311,178
Granted
Mar 6, 2007
Kind
B2
Abstract

A method for preparing cyclic urea compounds from at least an activated carbamic acid derivative containing an unprotected primary or secondary amine function, includes a cyclization step which consists in a reaction between the primary or secondary amine function and the carbamic acid function of the carbamic acid derivative(s).

Claims (25)

1. Cyclic urea compounds comprising a ring of at least 7 atoms, said cycle comprising at least one carboxylic amide function and at least one urea function, each amide and urea function being separated from the closest adjacent amide or urea function by at least one methylenic carbon atom.

2. The cyclic urea compounds of claim 1 , of formula (Ia):

in which the R 1 , R 2 , R 3 , R 4 , and R 5 groups can each and independently from one another represent:

a) a hydrogen;

b) a halogen;

c) the protected or non-protected side chain of an amino acid chosen from the natural or non-natural amino acids;

d) a linear or branched alkyl (C1–C20) group, non-substituted or substituted by one or more substituents which include: —COOR a , —CONHR a , —OR a , —NHR a , —NH(CO)R a , —NHCOOR a , an aryl or heteroaryl group, whose cyclic structure contains from 5–20 carbon atoms, one halogen atom, and one R′″CO— group, the R′″ group comprising from 1 to 10 carbon atoms, a nitrile, guanidino or nitro group;

e) one aryl group whose ring structure contains from 5 to 20 carbon atoms, substituted or non-substituted by the above-mentioned substituents, and by cyano or amidine groups;

f) an alkenyl or alkynyl group (C1–C6);

g) a sulfonyl group (R c SO 2 );

h) an acyl group (R c CO);

i) an OR b group;

j) an NH 2 group;

k) —COOR b ;

l) —CONHR b ;

m) —CH 2 CONH 2 ;

R a and R b representing, independently from one another, a hydrogen, an allyl, benzyl, t-butyl, fluorenylmethyl, benzyloxymethyl, tert-butyldimethylsilyl, 2-ethoxyethyl, methoxymethyl, 2-methoxyethoxymethyl, tetrahydropyran-2-yl, trhnethylsilyl, triethylsilyl, 2-(trimethylsilyl)ethyl, trityl, 2,2,2-trichioroethyl, tosyl, ortho-(or para)-nitrophenylsulfonyl, alkyl group having from 1 to 20 carbon atoms, or an aryl group whose ring structure contains from 5–20 carbon atoms;

R c representing an alkyl group having from 1 to 20 carbon atoms, or an aryl group whose ring structure contains from 5–20 carbon atoms, or a heteroaryl, arylalkyl or heteroarylalkyl group;

the R 1 , R 2 , R 3 and R 4 groups also being able to form the following intramolecular cyclizations:

1/cyclization between R 1 and R 2 and/or;

2/cyclization between R 3 and R 4 ;

said cyclic urea compounds able to be, when one or more asymmetric carbons are present in formula (Ia), independently, either of R configuration (rectus) or of S configuration (sinister).

3. The cyclic urea compounds of claim 2 , corresponding to formulae (Ib), (Ic), (Id), (Ie), (If), (Ig), (Ih):

wherein the R1 and R2 groups also being capable of forming an intramolecular cyclization,

said cyclic urea compounds able to be, when one or more asymmetric carbons are present in formulae (Ib) to (Ih), independently, either of R configuration (rectus) or of S configuration (sinister).

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 9, 2013
From: IMMUPHARMA (FRANCE) SA
To: UREKA SARL
Reel/Frame 030975/0283 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2006
From: NEOMPS
To: IMMUPHARMA (FRANCE) SA
Reel/Frame 017462/0103 →
CHANGE OF NAME Recorded Mar 11, 2005
From: NEOSYSTEM
To: NEOMPS
Reel/Frame 016381/0859 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 10, 2005
From: NEOSYSTEM
To: NEOMPS
Reel/Frame 015871/0111 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 26, 2003
From: GUICHARD, GILLES; PLAUE, SERGE; SEMETEY, VINCENT; SCHAFFNER, ARNAUD-PIERRE; BRIAND, JEAN-PAUL; RODRIGUEZ, MARC (DECEASED); GALAS-RODRIGUEZ, MARIE-CHRISTINE (LEGAL REPRESENTATIVE); RODRIGUEZ, PIERRE (LEGAL REPRESENTATIVE); RODRIGUEZ, ELISA (LEGAL REPRESENTATIVE); RODRIGUEZ, ROMAIN (LEGAL REPRESENTATIVE)
To: CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE; NEOSYSTEM
Reel/Frame 013786/0461 →