Hydrochloric Acid → (6S,9R)-6-(2,3-difluorophenyl)-3-(2,2,2-trifluoroethyl)-6,7,8,9-tetrahydro-5H-imidazo[1,2-a]azepin-9-amine
Reaction equation
Cl.[F:2][C:3]1[C:8]([F:9])=[CH:7][CH:6]=[CH:5][C:4]=1[C@H:10]1[CH2:16][N:15]2[C:17]([CH2:20][C:21]([F:24])([F:23])[F:22])=[CH:18][N:19]=[C:14]2[C@H:13]([NH:25]C(=O)OC(C)(C)C)[CH2:12][CH2:11]1>O1CCOCC1>[F:2][C:3]1[C:8]([F:9])=[CH:7][CH:6]=[CH:5][C:4]=1[C@H:10]1[CH2:16][N:15]2[C:17]([CH2:20][C:21]([F:24])([F:22])[F:23])=[CH:18][N:19]=[C:14]2[C@H:13]([NH2:25])[CH2:12][CH2:11]1Participants
4
Procedure
Hydrochloric acid (4.0 M in dioxane; 1 mL, 4.0 mmol) was added to a solution of tert-butyl [(6S,9R)-6-(2,3-difluorophenyl)-3-(2,2,2-trifluoroethyl)-6,7,8,9-tetrahydro-5H-imidazo[1,2-a]azepin-9-yl]carbamate (36 mg, 0.081 mmol) in dioxane (1 mL). After 18 h, the mixture was concentrated to give the hydrochloride salt of the title compound. MS 346.1 (M+1).
Workup
- concentrationthe mixture was concentrated
Sources & evidence
- ORD record
- ord-a711fa55d41e411ba16d49e6963f2db4
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08039460B2
Reaction notes
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