Hydrochloric Acid → HCID 58931116, compound
Reaction equation
C(O)C.O.[OH-].[Li+].C([O:9][C:10]([C:12]1[NH:38][C:15]2[N:16]=[CH:17][N:18]=[C:19]([O:20][C:21]3[CH:26]=[CH:25][C:24]([NH:27][C:28]([NH:30][C:31]4[CH:36]=[CH:35][C:34]([F:37])=[CH:33][CH:32]=4)=[O:29])=[CH:23][CH:22]=3)[C:14]=2[CH:13]=1)=[O:11])C.Cl>O>[F:37][C:34]1[CH:35]=[CH:36][C:31]([NH:30][C:28](=[O:29])[NH:27][C:24]2[CH:25]=[CH:26][C:21]([O:20][C:19]3[C:14]4[CH:13]=[C:12]([C:10]([OH:11])=[O:9])[NH:38][C:15]=4[N:16]=[CH:17][N:18]=3)=[CH:22][CH:23]=2)=[CH:32][CH:33]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 42.5 °C
Procedure
After adding 7 ml of ethanol, 7 ml of water and 31 mg of lithium hydroxide monohydrate to 75 mg of the 4-{4-[3-(4-fluorophenyl)ureido]phenoxy)-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid ethyl ester synthesized in Example 163 and stirring the mixture at 40-45° C. for 24 hours, it was neutralized with 2N HCl and concentrated to dryness to obtain 40 mg of the title compound.
Workup
- concentrationconcentrated to dryness
Sources & evidence
- ORD record
- ord-68aa816106d547c8a5063690ade9ed2f
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08372981B2
Reaction notes
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