Hydrochloric Acid → HCID 68976946, compound
Reaction equation
C(OC(=O)[NH:7][C@H:8]1[CH2:14][N:13]([CH2:15][C:16]([F:19])([F:18])[F:17])[C:12]2[CH:20]=[CH:21][CH:22]=[CH:23][C:11]=2[NH:10][C:9]1=[O:24])(C)(C)C.[ClH:26]>O1CCOCC1>[ClH:26].[NH2:7][C@@H:8]1[C:9](=[O:24])[NH:10][C:11]2[CH:23]=[CH:22][CH:21]=[CH:20][C:12]=2[N:13]([CH2:15][C:16]([F:19])([F:18])[F:17])[CH2:14]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In an analogous procedure to that described in Example 1d), the treatment of the [(S)-4-oxo-1-(2,2,2-trifluoro-ethyl)-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl]-carbamic acid tert-butyl ester with hydrochlorid acid (37%) in dioxane yielded the title compound as a light yellow solid; MS (m/e): 260 (M+H)+.
Sources & evidence
- ORD record
- ord-a7ed4e51c0fc4dc08bd5201328593940
- Source dataset
- uspto-grants-2008_08
- Patent number
- US07414049B2
Reaction notes
Loading…