Isoamylamine → HCID 67214309, compound
Reaction equation
[C:1]1([C:7]2[CH:8]=[C:9]([CH:13]=[CH:14][CH:15]=2)[C:10]([OH:12])=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:16]([NH2:21])[CH2:17][CH:18]([CH3:20])[CH3:19]>>[CH2:16]([NH:21][C:10](=[O:12])[C:9]1[CH:13]=[CH:14][CH:15]=[C:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[CH:8]=1)[CH2:17][CH:18]([CH3:20])[CH3:19]Participants
3
Procedure
Using Preparation Method 1, 3-phenylbenzoic acid was reacted with isoamylamine. The resulting reaction mixture was purified using SiO2 with CH2Cl2 100%. An off-white crystalline solid was obtained (61%). NMR 1H (ppm, CDCl3): 7.96 (s, 1H), 7.69 (d, J3=8.3 Hz, 2H), 7.59 (d, J3=7.2 Hz, 2H), 7.50-7.33 (m, 4H), 6.10 (br. s., 1H), 3.52-3.45 (m, 2H), 1.76-1.64 (m, 1H), 1.52 (quart., 2H), 0.95 (d, J3=6.6 Hz, 6H).
Workup
- customThe resulting reaction mixture
- customwas purified
- customAn off-white crystalline solid was obtained (61%)
Sources & evidence
- ORD record
- ord-f33012c2c6974d6ab59b680627780fc6
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07956216B2
Reaction notes
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