phenyl 3-(1-methyl-1H-tetraazol-5-yl)phenylcarbamate → HCID 11271867, compound

HRID 1592333Notes

Reaction equation

HRID 1592333 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([CH3:21])([CH3:20])[CH2:10][NH:11][CH2:12][CH:13]2[CH2:18][CH2:17][CH2:16][CH2:15][CH:14]2[NH2:19])=[CH:4][CH:3]=1.C1([O:28][C:29](=O)[NH:30][C:31]2[CH:36]=[CH:35][CH:34]=[C:33]([C:37]3[N:41]([CH3:42])[N:40]=[N:39][N:38]=3)[CH:32]=2)C=CC=CC=1>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][C:9]([CH3:21])([CH3:20])[CH2:10][NH:11][CH2:12][C@@H:13]2[CH2:18][CH2:17][CH2:16][CH2:15][C@H:14]2[NH:19][C:29]([NH:30][C:31]2[CH:36]=[CH:35][CH:34]=[C:33]([C:37]3[N:41]([CH3:42])[N:40]=[N:39][N:38]=3)[CH:32]=2)=[O:28])=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 22252681phenyl 3-(1-methyl-1H-tetraazol-5-yl)phenylcarbamateHCID 69423044HCID 69423044, compound

Product 1

HCID 11271867HCID 11271867, compound

Procedure

Using the amine from Step e and [3-(1-methyl-1H-tetrazol-5-yl)-phenyl]-carbamic acid phenyl ester, the titled compound was prepared by the methods desribed in Step d of Example 2.

Sources & evidence

ORD record
ord-6a1f3ed7c81846c2af50e5c15e5deb5e
Source dataset
uspto-grants-2007_11
Patent number
US07291744B2

Reaction notes

Loading…