Hydrochloric Acid → HCID 78320718, compound
Reaction equation
FC(F)(F)C(O)=O.[CH3:8][C@@H:9]1[CH2:13][CH2:12][CH2:11][N:10]1[CH2:14][CH2:15][C:16]1[CH:21]=[CH:20][C:19]([C:22]2[CH:27]=[CH:26][C:25]([C:28]3([C:33]([NH:35][C@@H:36]4[CH2:41][CH2:40][CH2:39][CH2:38][C@H:37]4[C:42]([O:44]CC)=[O:43])=[O:34])[CH2:32][CH2:31][CH2:30][CH2:29]3)=[CH:24][CH:23]=2)=[CH:18][CH:17]=1.[OH-].[Na+].Cl>O1CCOCC1>[CH3:8][C@@H:9]1[CH2:13][CH2:12][CH2:11][N:10]1[CH2:14][CH2:15][C:16]1[CH:17]=[CH:18][C:19]([C:22]2[CH:27]=[CH:26][C:25]([C:28]3([C:33]([NH:35][C@@H:36]4[CH2:41][CH2:40][CH2:39][CH2:38][C@H:37]4[C:42]([OH:44])=[O:43])=[O:34])[CH2:32][CH2:31][CH2:30][CH2:29]3)=[CH:24][CH:23]=2)=[CH:20][CH:21]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To (1R,2R)-ethyl 2-(1-(4′-(2-((R)-2-methylpyrrolidin-1-yl)ethyl)biphenyl-4-yl)cyclopentanecarboxamido)cyclohexanecarboxylate 2,2,2-trifluoroacetate (2.7 mg, 4.19 μmol) was added 5M sodium hydroxide (0.017 mL, 0.084 mmol). The reaction was stirred at room temperature overnight. The mixture was neutralized with 4M HCl in dioxane. The mixture was concentrated and triturated with acetonitrile to give the title compound. LCMS m/z=503.5 [M+H]+.
Workup
- concentrationThe mixture was concentrated
- customtriturated with acetonitrile
Sources & evidence
- ORD record
- ord-7fe41a6de3f84b7ba38247a09b34b71e
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09365511B2
Reaction notes
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