Acetic Acid → HCID 20036333, compound
Reaction equation
[C:1]([OH:4])(=[O:3])C.[CH:5]([OH:7])=O.C(OC(=O)C)(=O)C.[CH3:15][N:16]1[CH2:21][CH2:20][CH:19]([CH:22]2[C:28]3[CH:29]=[CH:30][CH:31]=[C:32]4[CH2:33][CH2:34][N:26]([C:27]=34)[C:25]3[CH:35]=[CH:36][CH:37]=[CH:38][C:24]=3[NH:23]2)[CH2:18][CH2:17]1>CO>[CH:1]([OH:4])=[O:3].[CH:5]([N:23]1[CH:22]([CH:19]2[CH2:20][CH2:21][N:16]([CH3:15])[CH2:17][CH2:18]2)[C:28]2[CH:29]=[CH:30][CH:31]=[C:32]3[CH2:33][CH2:34][N:26]([C:27]=23)[C:25]2[CH:35]=[CH:36][CH:37]=[CH:38][C:24]1=2)=[O:7]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of acetic acid (14.1 ml) and formic acid (14.8 ml) was prepared at -10° C. (methanol-ice) over a period of 1.5 hours. This solution, the mixed formic/acetic anhydride reagent, was added to 6-(1-methylpiperidin-4-yl)-1,2,6,7-tetrahydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine (16 gm) at room temperature in one portion. The mixture was stirred for 30 minutes. The resulting solution was treated with methanol (30 ml) and concentrated to an oil.
Workup
- concentrationconcentrated to an oil
Sources & evidence
- ORD record
- ord-dea03fe3c6b0448a85c54ba12d7407c7
- Source dataset
- uspto-grants-1989_06
- Patent number
- US04840947
Reaction notes
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