3-(3,5-Dimethoxyphenyl)prop-2-enoic acid → HCID 86604350, compound

HRID 1282521Notes

Reaction equation

HRID 1282521 reaction equation
[CH2:1]([N:5]([S:15]([C:18]1[CH:23]=[CH:22][C:21]([N+:24]([O-:26])=[O:25])=[CH:20][CH:19]=1)(=[O:17])=[O:16])[C@H:6]([C:12]([OH:14])=[O:13])[CH2:7][CH2:8][CH2:9][CH2:10][NH2:11])[CH:2]([CH3:4])[CH3:3].[CH3:27][O:28][C:29]1[CH:30]=[C:31]([CH:37]=[C:38]([O:40][CH3:41])[CH:39]=1)[CH:32]=[CH:33][C:34](O)=[O:35]>>[CH2:1]([N:5]([S:15]([C:18]1[CH:23]=[CH:22][C:21]([N+:24]([O-:26])=[O:25])=[CH:20][CH:19]=1)(=[O:17])=[O:16])[C@H:6]([C:12]([OH:14])=[O:13])[CH2:7][CH2:8][CH2:9][CH2:10][NH:11][C:34](=[O:35])[CH:33]=[CH:32][C:31]1[CH:30]=[C:29]([O:28][CH3:27])[CH:39]=[C:38]([O:40][CH3:41])[CH:37]=1)[CH:2]([CH3:4])[CH3:3]

Participants

3

Procedure

Nα-isobutyl-Nα-(4-nitrobenzenesulfonyl)-L-lysine was reacted with 3,5-dimethoxycinnamic acid under the conditions described in example 86 to yield 66% of the desired product.

Sources & evidence

ORD record
ord-293d8f395d084774b3f65b66ed3f2ffa
Source dataset
uspto-grants-2002_09
Patent number
US06455587B1

Reaction notes

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