Methyl-phenyl-carbamic Acid 4-(2-hydroxy-ethyl)-phenyl Ester → Methyl-phenyl-carbamic Acid 4-(2-tetrazol-1-yl-ethyl)-phenyl Ester
Reaction equation
O[CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][C:7]([O:10][C:11](=[O:20])[N:12]([CH3:19])[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[CH:6][CH:5]=1.[NH:21]1[CH:25]=[N:24][N:23]=[N:22]1>>[N:21]1([CH2:2][CH2:3][C:4]2[CH:9]=[CH:8][C:7]([O:10][C:11](=[O:20])[N:12]([CH3:19])[C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)=[CH:6][CH:5]=2)[CH:25]=[N:24][N:23]=[N:22]1Participants
3
Procedure
The title compound was prepared in 10% yield as an oil using methyl-phenyl-carbamic acid 4-(2-hydroxy-ethyl)-phenyl ester and tetrazole. NMR (400 MHz; CDCl3): δ 3.19 (t, 2H), 3.40 (br s, 3H), 3.47 (s, 1H), 4.61 (t, 2H), 6.98–7.07 (m, 4H), 7.25–7.42 (m, 5H), 8.26 (s, 1H); HPLC-MS: m/z=324.1 (M+1); Rt=3.36 min.
Sources & evidence
- ORD record
- ord-5ddef17d85ae4149806360dd98ed88ef
- Source dataset
- uspto-grants-2006_06
- Patent number
- US07067517B2
Reaction notes
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