Hydrochloric Acid → HCID 58421521, compound
Reaction equation
C[O:2][C:3]([C:5]1[S:30][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[CH2:27][CH2:26][CH2:25][CH2:24][C@H:23]3[O:28][CH3:29])[C:7]=2[C:6]=1[CH3:31])=[O:4].[OH-].[Na+].C1COCC1.Cl>O.CO>[F:20][C:17]1[CH:18]=[CH:19][C:14]([NH:13][C:12]2[C:7]3[C:6]([CH3:31])=[C:5]([C:3]([OH:4])=[O:2])[S:30][C:8]=3[N:9]=[CH:10][N:11]=2)=[C:15]([O:21][C@@H:22]2[CH2:27][CH2:26][CH2:25][CH2:24][C@H:23]2[O:28][CH3:29])[CH:16]=1Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 1.75 g 4-[4-fluoro-2-((1R,2R)-2-methoxy-cyclohexyloxy)-phenylamino]-5-methyl-thieno[2,3-d]pyrimidine-6-carboxylic acid methyl ester, 4M sodium hydroxide solution, 20 ml THF and 20 ml MeOH was stirred at rt overnight. The reaction mixture was acidified by addition of hydrochloric acid, diluted with 80 ml water and filtered. The solid was washed with water and dried in vacuo at 65° C.
Workup
- filtrationfiltered
- washThe solid was washed with water
- customdried in vacuo at 65° C.
Sources & evidence
- ORD record
- ord-c3da073d481647bb8c695341d31dd7e3
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08754079B2
Reaction notes
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