1,3-Benzodioxole-5-carbonyl chloride → N-(2-methylheptan-4-yl)benzo[d][1,3]dioxole-5-carboxamide
Reaction equation
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10](Cl)=[O:11])=[CH:9][C:4]=2[O:3][CH2:2]1.[CH3:13][CH:14]([CH2:16][CH:17]([NH2:21])[CH2:18][CH2:19][CH3:20])[CH3:15]>>[CH3:13][CH:14]([CH2:16][CH:17]([NH:21][C:10]([C:8]1[CH:7]=[CH:6][C:5]2[O:1][CH2:2][O:3][C:4]=2[CH:9]=1)=[O:11])[CH2:18][CH2:19][CH3:20])[CH3:15]Participants
3
Procedure
Prepared in a similar manner to example 1 using benzo[d][1,3]dioxole-5-carbonyl chloride and 2-methylheptan-4-amine (example 2a). 1H NMR (500 MHz, CDCl3): δ 0.93 (m, 9H); 1.38 (m, 5H); 1.53 (m, 1H); 1.66 (m, 1H); 4.21 (m, 1H); 5.61 (d, 1H); 6.01 (s, 2H); 6.82 (d, 1H); 7.26 (m, 2H). MS (278, M+H).
Sources & evidence
- ORD record
- ord-01f8007abead4b47b45ea3db47d2f019
- Source dataset
- uspto-grants-2012_04
- Patent number