3-Acetoxy-2-naphthoic acid → HCID 59852599, compound
Reaction equation
[C:1]([O:4][C:5]1[C:6]([C:15]([OH:17])=O)=[CH:7][C:8]2[C:13]([CH:14]=1)=[CH:12][CH:11]=[CH:10][CH:9]=2)(=[O:3])[CH3:2].[CH3:18][O:19][C:20]1[C:25]([C:26]2[CH:31]=[CH:30][C:29]([N+:32]([O-:34])=[O:33])=[CH:28][CH:27]=2)=[CH:24][C:23]([CH2:35][CH2:36][NH2:37])=[CH:22][CH:21]=1>>[CH3:18][O:19][C:20]1[C:25]([C:26]2[CH:31]=[CH:30][C:29]([N+:32]([O-:34])=[O:33])=[CH:28][CH:27]=2)=[CH:24][C:23]([CH2:35][CH2:36][NH:37][C:15]([C:6]2[C:5]([O:4][C:1](=[O:3])[CH3:2])=[CH:14][C:13]3[C:8]([CH:7]=2)=[CH:9][CH:10]=[CH:11][CH:12]=3)=[O:17])=[CH:22][CH:21]=1Participants
3
Procedure
Acetic acid 3-[2-(6-methoxy-4′-nitro-biphenyl-3-yl)-ethylcarbamoyl]-naphthalen-2-yl ester (108 mg) was prepared from 3-Acetoxy-naphthalene-2-carboxylic acid (58 mg, 0.25 mmol) and 2-(6-Methoxy-4′-nitro-biphenyl-3-yl)-ethylamine (68 mg, 0.25 mmol following the general procedure A.
Sources & evidence
- ORD record
- ord-9edeae5b37a94032a94a80a4086521fe
- Source dataset
- uspto-grants-2008_12
- Patent number
- US07459472B2
Reaction notes
Loading…