N-Methylbenzylamine → HCID 58933889, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([C:12]([OH:14])=O)[CH:6]=[CH:5]2.[CH3:15][NH:16][CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[CH2:17]([N:16]([CH3:15])[C:12]([C:7]1[CH:6]=[CH:5][C:4]2[C:9](=[CH:10][CH:11]=[C:2]([OH:1])[CH:3]=2)[CH:8]=1)=[O:14])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1Participants
3
Procedure
The title compound was synthesised from 6-hydroxy-2-naphtoic acid (commercially available) and N-methylbenzylamine (commercially available) according to the procedure described for Example A. MS (m/e): 290.1 (MH−, 100%)
Sources & evidence
- ORD record
- ord-6afdcf655a14436f946a9967afc02018
- Source dataset
- uspto-grants-2007_08
- Patent number
- US07259158B2
Reaction notes
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