Borane → HCID 68146681, compound
Reaction equation
[CH3:1][N:2]1[C:8]2[CH:9]=[CH:10][C:11]([C:13]([F:16])([F:15])[F:14])=[CH:12][C:7]=2[C:6](=O)[N:5]2[CH2:18][CH2:19][CH2:20][CH:4]2[C:3]1=[O:21].B>O1CCCC1>[CH3:1][N:2]1[C:8]2[CH:9]=[CH:10][C:11]([C:13]([F:16])([F:14])[F:15])=[CH:12][C:7]=2[CH2:6][N:5]2[CH2:18][CH2:19][CH2:20][CH:4]2[C:3]1=[O:21]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
If 1,2,3,11a-tetrahydro-10-methyl-7 -trifluoromethyl-5 H-pyrrolo[2,1-c] [1,4] benzodiazepin-5,11(10H)-dione (prepared from proline and 5-trifluoromethyl N-methylisatoic anhydride as described in Example 1) is treated with 1M borane in tetrahydrofuran as described in Example 1, the above compound is obtained.
Workup
- customthe above compound is obtained
Sources & evidence
- ORD record
- ord-ffe2def51f494cd1824b3615fa0ad198
- Source dataset
- uspto-grants-1976_03
- Patent number
- US03947408
Reaction notes
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