Hydrochloric Acid → HCID 117699115, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][C:8]([NH:10][C:11]2[CH:16]=[CH:15][C:14]([N:17]3[C:23](=[O:24])[CH2:22][C:21](=[O:25])[NH:20][C:19]4[C:26]5[C:31]([CH:32]=[CH:33][C:18]3=4)=[CH:30][CH:29]=[CH:28][CH:27]=5)=[CH:13][CH:12]=2)=[O:9])[CH:2]=1.[ClH:34]>C(Cl)(Cl)Cl.C(OCC)(=O)C>[ClH:34].[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][C:8]([NH:10][C:11]2[CH:16]=[CH:15][C:14]([N:17]3[C:23](=[O:24])[CH2:22][C:21](=[O:25])[NH:20][C:19]4[C:26]5[C:31]([CH:32]=[CH:33][C:18]3=4)=[CH:30][CH:29]=[CH:28][CH:27]=5)=[CH:13][CH:12]=2)=[O:9])[CH:2]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
5-[4-[(3-Pyridylacetyl)amino]phenyl]-1H-naphtho[1,2-b][1,4]diazepine-2,4(3H,5H)-dione (6.2 mg, 0.014 mmol) was dissolved in chloroform (6 mL), the solution was added with a 4 M solution of hydrogen chloride in ethyl acetate (0.01 mL), and the solvent was evaporated under reduced pressure. The residue was concentrated from ethyl acetate under reduced pressure, and then washed with ethyl acetate to obtain the title compound (4.8 mg, yield 71%) as pale brown powder.
Workup
- customthe solvent was evaporated under reduced pressure
- concentrationThe residue was concentrated from ethyl acetate under reduced pressure
- washwashed with ethyl acetate
Sources & evidence
- ORD record
- ord-4c6259c8be9d4f59bec54e9e00635a50
- Source dataset
- uspto-grants-2016_07
- Patent number
- US09382236B2
Reaction notes
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