Hydrochloric Acid → HCID 58421739, compound
Reaction equation
C[O:2][C:3]([C:5]1[S:35][C:8]2[N:9]=[CH:10][N:11]=[C:12]([NH:13][C:14]3[CH:19]=[CH:18][C:17]([F:20])=[CH:16][C:15]=3[O:21][C@H:22]3[CH2:26][CH2:25][CH2:24][C@@H:23]3[NH:27][C:28]([O:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[O:29])[C:7]=2[C:6]=1[CH3:36])=[O:4].[OH-].[Na+].Cl>CO.O>[C:31]([O:30][C:28]([NH:27][C@H:23]1[CH2:24][CH2:25][CH2:26][C@@H:22]1[O:21][C:15]1[CH:16]=[C:17]([F:20])[CH:18]=[CH:19][C:14]=1[NH:13][C:12]1[C:7]2[C:6]([CH3:36])=[C:5]([C:3]([OH:4])=[O:2])[S:35][C:8]=2[N:9]=[CH:10][N:11]=1)=[O:29])([CH3:34])([CH3:32])[CH3:33]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 2.4 g (1S,2S) 4-[2-(2-tert-butoxycarbonylamino-cyclopentyloxy)-4-fluoro-phenylamino]-5-methyl thieno[2,3-d]pyrimidine-6-carboxylic acid methyl ester and 20 ml 1M sodium hydroxide solution in 50 ml MeOH was stirred at rt overnight. To the reaction mixture was added 20 ml 1M hydrochloric acid until a pH range of 2-3 was reached. The mixture was diluted with water and filtrated. The solid was dried in vacuo at 50° C.
Workup
- filtrationfiltrated
- customThe solid was dried in vacuo at 50° C.
Sources & evidence
- ORD record
- ord-0e034265de37469e9188ffcbc2222d58
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08754079B2
Reaction notes
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