N-Butyl-N-(1-phenyltetrazol-5-yl)amine → 4-N-Butyl-N-(1-phenyltetrazol-5-yl)aminomethyl-2-(2-methylphenyl)benzoic acid methyl ester
Reaction equation
[CH3:1][O:2][C:3](=[O:19])[C:4]1[CH:9]=[CH:8][C:7](CBr)=[CH:6][C:5]=1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[CH3:18].[CH2:20]([NH:24][C:25]1[N:29]([C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)[N:28]=[N:27][N:26]=1)CCC>>[CH3:1][O:2][C:3](=[O:19])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH2:20][NH:24][CH:25]2[N:29]([C:30]3[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=3)[N:28]=[N:27][N:26]2[CH2:3][CH2:4][CH2:5][CH3:6])[C:5]=1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[CH3:18]Participants
3
Procedure
The desired compound was prepared according to the method of Example 1174B starting with 4-bromomethyl-2-(2-methylphenyl)benzoic acid methyl ester, prepared as in Example 1178A-D, and the compound from Example 1180A.
Sources & evidence
- ORD record
- ord-246e7f2057b14ab5af73a3be02dbbee3
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06310095B1
Reaction notes
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