alpha-Hydroxytriazolam → HCID 70359543, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:11]3[C:12]([CH2:15][OH:16])=[N:13][N:14]=[C:10]3[CH2:9][N:8]=[C:7]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[Cl:23])[C:6]=2[CH:24]=1.[C:25]([O:30]C(=O)CCC)(=[O:29])[CH2:26][CH2:27][CH3:28]>O>[C:25]([OH:30])(=[O:29])[CH2:26][CH2:27][CH3:28].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:11]3[C:12]([CH2:15][OH:16])=[N:13][N:14]=[C:10]3[CH2:9][N:8]=[C:7]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[Cl:23])[C:6]=2[CH:24]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In a manner similar to Example 12, a mixture of 8-chloro-1-(hydroxymethyl)-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine and butyric anhydride was heated on the water bath to give 8-chloro-1-hydroxymethyl-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine butyrate (ester).
Sources & evidence
- ORD record
- ord-e7b0f2d82d1e45ec9482b63f42e0f703
- Source dataset
- uspto-grants-1990_02
- Patent number
- US04902794
Reaction notes
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