Hydrochloric Acid → HCID 58413161, compound
Reaction equation
C[O:2][C:3]([C:5]1[S:27][C:8]2[N:9]=[CH:10][N:11]=[C:12]([NH:13][C:14]3[C:15]([O:20][C@@H:21]4[CH2:26][CH2:25][CH2:24][O:23][CH2:22]4)=[N:16][CH:17]=[CH:18][CH:19]=3)[C:7]=2[C:6]=1[CH3:28])=[O:4].CO.[OH-].[Na+].Cl>O.C1COCC1>[CH3:28][C:6]1[C:7]2[C:12]([NH:13][C:14]3[C:15]([O:20][C@@H:21]4[CH2:26][CH2:25][CH2:24][O:23][CH2:22]4)=[N:16][CH:17]=[CH:18][CH:19]=3)=[N:11][CH:10]=[N:9][C:8]=2[S:27][C:5]=1[C:3]([OH:4])=[O:2]Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 1.4 g (3.14 mmol) 5-methyl-4-{2-[(R)-(tetrahydro-pyran-3-yl)oxy]-pyridin-3-ylamino}-thieno[2,3-d]pyrimidine-6-carboxylic acid methyl ester, 20 ml methanol, 7 ml THF and 6.29 ml sodium hydroxid solution (1 M) was stirred at room temperature for 48 hours. Then 6.3 ml hydrochloric acid solution (1M) were added followed by addition of water. The mixture was filtered. The solid was washed with water and diisopropylether and dried in an oven (vacuo).
Workup
- filtrationThe mixture was filtered
- washThe solid was washed with water and diisopropylether
- customdried in an oven (vacuo)
Sources & evidence
- ORD record
- ord-a3840c4d87a74ed19b0b948ca86a5636
- Source dataset
- uspto-grants-2014_02
- Patent number
- US08648068B2
Reaction notes
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