IP Library Patent Application 14774522
Patent Application
App. No. 14/774,522

PROCESSES FOR PREPARING TETRAHYDROISOQUINOLINES

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Patent No.
US None
App. No.
14/774,522
Abstract

Disclosed are processes for preparing tetrahydroisoquinolines, intermediates useful in the preparation of tetrahydroisoquinolines, processes for preparing such intermediates, and compositions comprising the tetrahydroisoquinolines and other compounds, e.g, intermediates and by-products of the processes described herein. Pharmaceutical compositions comprising tetrahydroisoquinolines, methods of using tetrahydroisoquinolines in the treatment of depression are also disclosed.

Claims (33)

1 . A composition comprising a compound having the following formula:

and a compound having the following formula:

said Compound 2 present in an amount of from about 1 ppm to less than 1.0 wt % based on the weight of Compound 1.

2 . The composition of claim 1 wherein the amount of

is less than about 1500 ppm based on the weight of Compound 1.

3 . The composition of claim 2 wherein the amount of

is less than about 500 ppm based on the weight of Compound 1.

4 . A composition comprising a compound having the following formula:

and a compound having the following formula:

said Compound 3 present in an amount of from about 1 ppm to less than 1.0 wt % based on the weight of Compound 1.

5 . A composition of claim 4 wherein the amount of

is less than about 1500 ppm based on the weight of Compound 1.

6 . A composition of claim 5 wherein the amount of

is less than about 500 ppm based on the weight of Compound 1.

7 . A composition of claim 1 further comprising a compound having the following formula:

said Compound 3 present in an amount of from about 1 ppm to less than 1.0 wt % based on the weight of Compound 1.

8 . A compound having the formula:

wherein

R 1 is selected from the group consisting of B(OH) 2 , B(OR 3 ) 2 , B(O 2 COR 3 ) 2 , and —BF 3 K;

R 2 is selected from the group consisting of H, CH 3 , CH 2 CH 2 SiMe 3 , benzyl, diphenylmethyl, p-methoxybenzyl, 3,4-dimethoxybenzyl, COOC(CH 3 ) 3 ; COOCH 3 , COOCH 2 CH 3 , COOAllyl, COObenzyl, COO-p-methoxybenzyl, COOCH 2 CH 2 SiMe 3 , 9-Fluorenylmethyloxycarbonyl, COOCH 2 CH 2 CCl 3 , COH, COMe, COPh, and COCF 3 , and

R 3 is selected from the group consisting of alkyl, aryl and heteroaryl;

and/or salts thereof.

9 . A composition of claim 1 wherein Compound 1 is in the form of Compound 1-(4S).

10 . A composition of claim 1 wherein Compound 1 is in the crystalline form of Form N-1.

11 . A composition of claim 9 in the form of a tablet or capsule comprising from about 0.10 to 2.0 mg of Compound 1-(4S).

12 . A composition of claim 9 in the form of a tablet or capsule comprising from about 0.10 to 2.0 mg of Compound 1-(4S) further comprising a pharmaceutically acceptable additive.

13 . A composition of claim 9 in the form of a tablet or capsule comprising from about 0.10 to 2.0 mg of Compound 1-(4S) further comprising a pharmaceutically acceptable additive, the composition providing a total blood plasma concentration profile of Compound 1-(4S), as measured by AUC at 24 hours after an initial dose of the composition, that is at least greater than about 50% of the total blood plasma concentration as measured by AUC at 24 hours of an initial dose of an orally administered solution comprising Compound 1-(4S).

14 . A composition of claim 9 in the form of a tablet or capsule comprising from about 0.10 to 2.0 mg of Compound 1-(4S) further comprising a pharmaceutically acceptable additive, the composition providing a blood plasma concentration profile after an initial dose of the composition has a Cmax of Compound 1-(4S) that is at least greater than about 40% of the Cmax of an orally administered solution comprising Compound 1-(4S).

15 . A method of treating depression comprising administering to a patient in need thereof the composition of claim 1 .

16 . A method of claim 15 wherein Compound 1 is in the form of Compound 1-(4S).

17 . A method of treating a major depressive episode in adult patients with major depressive disorder who have experienced inadequate response to separate trials of adequate dose and duration of two antidepressants from different classes in the current episode, comprising administering to the patient a composition comprising Compound 1-(4S).

18 . A method of treating depression comprising administering to a patient in need thereof a composition of claim 9 wherein a total blood plasma concentration profile of Compound 1-(4S) is provided, as measured by AUC at 24 hours after an initial dose of the composition, that is at least greater than about 50% of the total blood plasma concentration as measured by AUC at 24 hours of an initial dose of an orally administered solution comprising Compound 1-(4S).

19 . A method of treating depression comprising administering to a patient in need thereof a composition of claim 9 wherein a blood plasma concentration profile after an initial dose of the composition has a Cmax of Compound 1-(4S) that is at least greater than about 40% of the Cmax of an orally administered solution comprising Compound 1-(4S).

Assignments (5)
ASSIGNMENT OF SECURITY INTEREST IN INTELLECTUAL PROPERTY, RECORDED ON SEPTEMBER 1, 2017, AT REEL/FRAME 043746/0621 Recorded Mar 17, 2025
From: BARCLAYS BANK PLC, AS EXISTING AGENT
To: APOLLO ADMINISTRATIVE AGENCY LLC, AS SUCCESSOR AGENT
Reel/Frame 070531/0279 →
SECURITY INTEREST Recorded Sep 6, 2021
From: CURIA GLOBAL, INC. (FKA ALBANY MOLECULAR RESEARCH, INC.); CURIA MASSACHUSETTS, INC. (FKA AMRI BURLINGTON, INC.); CURIA WISCONSIN, INC. (FKA CEDARBURG PHARMACEUTICALS, INC.); CURIA INDIANA, LLC (FKA AMRI SSCI, LLC); CURIA NEW MEXICO, LLC (FKA OSO BIOPHARMACEUTICALS MANUFACTURING, LLC); CURIA IP HOLDINGS, LLC
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 057423/0665 →
RELEASE OF SECURITY INTEREST Recorded Oct 29, 2020
From: MORGAN STANLEY SENIOR FUNDING, INC., AS COLLATERAL AGENT
To: ALBANY MOLECULAR RESEARCH, INC.; AMRI BURLINGTON, INC.; CEDARBURG PHARMACEUTICALS, INC.; EUTICALS INC.; OSO BIOPHARMACEUTICALS MANUFACTURING, LLC
Reel/Frame 054252/0687 →
FIRST LIEN SECURITY AGREEMENT Recorded Sep 1, 2017
From: ALBANY MOLECULAR RESEARCH, INC.; AMRI BURLINGTON, INC.; CEDARBURG PHARMACEUTICALS, INC.; EUTICALS INC.; OSO BIOPHARMACEUTICALS MANUFACTURING, LLC-BY ITS SOLE MEMBER: ALO ACQUISITION LLC
To: BARCLAYS BANK, PLC AS COLLATERAL AGENT
Reel/Frame 043746/0621 →
SECOND LIEN SECURITY AGREEMENT Recorded Sep 1, 2017
From: ALBANY MOLECULAR RESEARCH, INC.; AMRI BURLINGTON, INC.; CEDARBURG PHARMACEUTICALS, INC.; EUTICALS INC.; OSO BIOPHARMACEUTICALS MANUFACTURING LLC-BY ITS SOLE MEMBER:ALO ACQUISITION LLC
To: MORGAN STANLEY SENIOR FUNDING, INC.
Reel/Frame 043746/0657 →