HCID 43162944, compound → 1298047-69-4

HRID 1918388Notes

Reaction equation

HRID 1918388 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:10]2[CH:11]=[N:12][CH:13]=[C:14]([CH:18]=2)[C:15]([OH:17])=O)[CH:5]=[CH:6][C:7]=1[O:8][CH3:9].[CH3:19][O:20][C:21]([C:23]1([NH2:31])[CH2:28][CH2:27][CH:26]([CH2:29][CH3:30])[CH2:25][CH2:24]1)=[O:22]>>[CH3:19][O:20][C:21]([C:23]1([NH:31][C:15]([C:14]2[CH:13]=[N:12][CH:11]=[C:10]([C:4]3[CH:5]=[CH:6][C:7]([O:8][CH3:9])=[C:2]([Cl:1])[CH:3]=3)[CH:18]=2)=[O:17])[CH2:28][CH2:27][CH:26]([CH2:29][CH3:30])[CH2:25][CH2:24]1)=[O:22]

Participants

3

Procedure

The title compound was synthesized from 5-(3-Chloro-4-methoxy-phenyl)-nicotinic acid and 1-Amino-4-ethyl-cyclohexanecarboxylic acid methyl ester in analogy to example 126, step 4.

Sources & evidence

ORD record
ord-9cf4b8130c1f4cd1b1060b19ecec0d8c
Source dataset
uspto-grants-2013_12
Patent number
US08618304B2

Reaction notes

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