Isopropylamine → 3-[Benzyl-(pyridine-3-sulfonyl)-amino]-N-isopropyl-benzamide
Reaction equation
[CH2:1]([N:8]([S:18]([C:21]1[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=1)(=[O:20])=[O:19])[C:9]1[CH:10]=[C:11]([CH:15]=[CH:16][CH:17]=1)[C:12]([OH:14])=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH:27]([NH2:30])([CH3:29])[CH3:28]>>[CH2:1]([N:8]([S:18]([C:21]1[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=1)(=[O:19])=[O:20])[C:9]1[CH:10]=[C:11]([CH:15]=[CH:16][CH:17]=1)[C:12]([NH:30][CH:27]([CH3:29])[CH3:28])=[O:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
3[Benzyl-(pyridine-3-sulfonyl)-amino]-N-isopropyl-benzamide was prepared from 3-[benzyl-(pyridine-3-sulfonyl)-amino]-benzoic acid and isopropylamine according to the method described for Example 2. HPLC retention time 5.46 min. Mass spectrum (APCI+) m/z 410 (M+H).
Sources & evidence
- ORD record
- ord-2d244a1d0b624c608e0375dca85688e2
- Source dataset
- uspto-grants-2015_07
- Patent number
- US09073834B2
Reaction notes
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