Succinic Acid → HCID 67463174, compound
Reaction equation
[Cl:1][C:2]1[CH:12]=[CH:11][C:5]2[CH2:6][CH2:7][NH:8][CH2:9][CH2:10][C:4]=2[C:3]=1[NH:13][CH2:14][C:15]1[CH:20]=[CH:19][C:18]([CH2:21][S:22]([CH2:25][C:26]([CH3:29])([CH3:28])[CH3:27])(=[O:24])=[O:23])=[CH:17][CH:16]=1.[C:30]([OH:37])(=[O:36])[CH2:31][CH2:32][C:33]([OH:35])=[O:34]>CO>[C:30]([OH:37])(=[O:36])[CH2:31][CH2:32][C:33]([OH:35])=[O:34].[Cl:1][C:2]1[CH:12]=[CH:11][C:5]2[CH2:6][CH2:7][NH:8][CH2:9][CH2:10][C:4]=2[C:3]=1[NH:13][CH2:14][C:15]1[CH:20]=[CH:19][C:18]([CH2:21][S:22]([CH2:25][C:26]([CH3:29])([CH3:28])[CH3:27])(=[O:24])=[O:23])=[CH:17][CH:16]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Dissolve 7-chloro-6-[4-(2,2-dimethyl-propanesulfonylmethyl)-benzylamino]-2,3,4,5-tetrahydro-1H-benzo[d]azepine (316 mg, 0.726 mmol) in methanol (10 mL) and add succinic acid (86 mg, 0.726 mmol). Stir the mixture for 2 h. Concentrate the mixture in vacuo and dry under high vacuum at 50° C. to obtain the title compound (380 mg, 94%). MS (APCI+) m/z: 435 (M+H)+.
Workup
- concentrationConcentrate the mixture in vacuo
- customdry under high vacuum at 50° C.
Sources & evidence
- ORD record
- ord-054abe6054ed4daaa95b223a5760e573
- Source dataset
- uspto-grants-2014_03
- Patent number
- US08680091B2
Reaction notes
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