Hydrochloric Acid → HCID 66755065, compound
Reaction equation
[ClH:1].C(OC(=O)[NH:8][C:9]([C:12]1[O:16][N:15]=[C:14]([CH:17]2[CH2:22][CH:21]([C:23]3[CH:28]=[CH:27][C:26]([C:29]([F:32])([F:31])[F:30])=[CH:25][CH:24]=3)[CH2:20][N:19]([C:33]([N:35]3[CH2:40][CH2:39][O:38][CH2:37][CH2:36]3)=[O:34])[CH2:18]2)[N:13]=1)([CH3:11])[CH3:10])(C)(C)C>O1CCOCC1>[ClH:1].[NH2:8][C:9]([C:12]1[O:16][N:15]=[C:14]([CH:17]2[CH2:22][CH:21]([C:23]3[CH:28]=[CH:27][C:26]([C:29]([F:31])([F:32])[F:30])=[CH:25][CH:24]=3)[CH2:20][N:19]([C:33]([N:35]3[CH2:40][CH2:39][O:38][CH2:37][CH2:36]3)=[O:34])[CH2:18]2)[N:13]=1)([CH3:11])[CH3:10]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
0.12 ml (0.50 mmol) of a 4N solution of hydrogen chloride in dioxane was added to a solution of 29 mg (about 0.05 mmol) of the compound from Example 86A in 0.2 ml of dioxane. The reaction mixture was stirred at room temperature for 20 hours. The mixture was then concentrated to dryness under reduced pressure and dried until the weight remained constant. Yield: 24 mg (96% of theory).
Workup
- concentrationThe mixture was then concentrated to dryness under reduced pressure
- customdried until the weight
Sources & evidence
- ORD record
- ord-dc98869aad1d40e1bf6ec8e142177480
- Source dataset
- uspto-grants-2012_02
- Patent number
- US08119663B2
Reaction notes
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