Dipropylamine → HCID 20025791, compound
Reaction equation
[CH2:1]([NH:4][CH2:5][CH2:6][CH3:7])[CH2:2][CH3:3].Cl[CH2:9][CH2:10][CH2:11][CH2:12][O:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1/[CH:20]=[CH:21]/[C:22]1[S:23][C:24]2[CH:30]=[CH:29][CH:28]=[CH:27][C:25]=2[N:26]=1>>[CH2:1]([N:4]([CH2:5][CH2:6][CH3:7])[CH2:9][CH2:10][CH2:11][CH2:12][O:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1/[CH:20]=[CH:21]/[C:22]1[S:23][C:24]2[CH:30]=[CH:29][CH:28]=[CH:27][C:25]=2[N:26]=1)[CH2:2][CH3:3]Participants
3
Procedure
Reaction of this product (5.0 g, 14.5 mmol) with dipropylamine produced 2.1 g (35% yield) of the named compound as the HCl salt, mp 155°-156° C. IR(KBr): 3400, 1600 cm-1. MS: 409(MH+). 1H NMR (CD3OD): δ 8.19-6.99 (m, 10H), 4.10 (t, J=5.2 Hz, 2H), 3.12(m, 6H), 1.85(m, 8H), 1.02 (m, 6H).
Sources & evidence
- ORD record
- ord-e15ae4b72b1c4bc89ec8fb7fa9b4b461
- Source dataset
- uspto-grants-1989_08
- Patent number
- US04861897
Reaction notes
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