Borane → HCID 21449050, compound
Reaction equation
[NH2:1][CH:2]([CH3:25])[CH2:3][C:4]1[N:8]2[C:9]3[CH:23]=[CH:22][C:21]([Cl:24])=[CH:20][C:10]=3[C:11]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[N:12][CH2:13][C:7]2=[N:6][N:5]=1.B>O1CCCC1>[NH2:1][CH:2]([CH3:25])[CH2:3][C:4]1[N:8]2[C:9]3[CH:23]=[CH:22][C:21]([Cl:24])=[CH:20][C:10]=3[CH:11]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[NH:12][CH2:13][C:7]2=[N:6][N:5]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In the manner given in Example 23 a mixture of 1-(2-aminopropyl)-8-chloro-6-phenyl-4H-s-triazolo[4,3-a][1,4]-benzodiazepine and tetrahydrofuran was treated with borane to give 1-(2-aminopropyl)-8-chloro-5,6-dihydro-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine.
Sources & evidence
- ORD record
- ord-c43501de3a1c4b0086ccac316772f3e8
- Source dataset
- uspto-grants-1977_03
- Patent number
- US04012413
Reaction notes
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