Diisopropylaniline → HCID 10672037, compound

HRID 1756907Notes

Reaction equation

[CH2:1]([N:13]1[N:17]=[N:16][C:15]([CH2:18][CH2:19][C:20]([OH:22])=O)=[N:14]1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[CH3:23][CH:24]([C:26]1[CH:32]=[CH:31][CH:30]=[C:29]([CH:33]([CH3:35])[CH3:34])[C:27]=1[NH2:28])[CH3:25]>>[CH3:35][CH:33]([C:29]1[CH:30]=[CH:31][CH:32]=[C:26]([CH:24]([CH3:25])[CH3:23])[C:27]=1[NH:28][C:20](=[O:22])[CH2:19][CH2:18][C:15]1[N:16]=[N:17][N:13]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12])[N:14]=1)[CH3:34]

Participants

Reactant 2

HCID 32484Diisopropylaniline

HCID 10804921HCID 10804921, compound

Product 1

HCID 10672037HCID 10672037, compound

Procedure

In a manner similar to Example 34, 2-dodecyl-2H-tetrazole-5-propanoic acid was condensed with 2,6-bis(1-methylethyl)aniline to give the title compound, mp 41°-43° C.

Sources & evidence

ORD record: ord-de37a56fb74e46babf170f64120b5058
Source dataset: uspto-grants-1995_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05441975

Reaction notes

Loading…