1-Iodohexane → HCID 21488933, compound
Reaction equation
[CH2:1]([N:8]([CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[CH2:9][C:10]([C:12]1[CH:13]=[CH:14][C:15]([O:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26]C)=[C:16]([CH:20]=1)[C:17]([NH2:19])=[O:18])=[O:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(I)CCCCC>>[CH2:1]([N:8]([CH2:28][C:29]1[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=1)[CH2:9][C:10]([C:12]1[CH:13]=[CH:14][C:15]([O:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])=[C:16]([CH:20]=1)[C:17]([NH2:19])=[O:18])=[O:11])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
3(a) 5-(N,N-dibenzylglycyl)-2-hexyloxybenzamide, m.p. 92°-94°, 53% (hexyl iodide).
Sources & evidence
- ORD record
- ord-74f059b45b644824a94b4e61ca1f294e
- Source dataset
- uspto-grants-1976_12
- Patent number
- US04000193
Reaction notes
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