Diisopropylaniline → (+/-)-5-dodecyl-alpha-pentyl-N-(2,4,6-trimethoxyphenyl)-2H-tetrazole-2-acetamide
Reaction equation
[CH2:1]([C:13]1[N:14]=[N:15][N:16]([CH:18]([CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[C:19]([OH:21])=O)[N:17]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].C(C1N=NN(CC(O)=O)N=1)CCCCCCCCC.[CH3:46][O:47][C:48]1[CH:54]=[C:53]([O:55][CH3:56])[CH:52]=[C:51]([O:57][CH3:58])[C:49]=1[NH2:50].C(C1C=CC=C(C(C)C)C=1N)(C)C>>[CH2:1]([C:13]1[N:14]=[N:15][N:16]([CH:18]([CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[C:19]([NH:50][C:49]2[C:51]([O:57][CH3:58])=[CH:52][C:53]([O:55][CH3:56])=[CH:54][C:48]=2[O:47][CH3:46])=[O:21])[N:17]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]Participants
5
Procedure
When in the general procedure of Example 88 an appropriate amount of (±)-5-dodecyl-α-pentyl-2H-tetrazole-2-acetic acid was substituted for 5-decyl-2H-tetrazole-2-acetic acid and 2,4,6-trimethoxyaniline was substituted for 2,6-diisopropylaniline, the title compound was obtained, mp 152°-155° C.
Sources & evidence
- ORD record
- ord-a016e6b756f04a429050aab889041458
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05441975
Reaction notes
Loading…