HCID 21558567, compound → HCID 135783924, compound

HRID 1578738Notes

Reaction equation

HRID 1578738 reaction equation
Cl[C:2]1[C:10]2[NH:9][C:8]([C:11]([F:14])([F:13])[F:12])=[N:7][C:6]=2[C:5]([N+:15]([O-:17])=[O:16])=[CH:4][C:3]=1[C:18]#[N:19].[CH2:20]([CH:22]1[CH2:25][CH2:24][CH:23]1[NH2:26])[CH3:21]>>[CH2:20]([CH:22]1[CH2:25][CH2:24][CH:23]1[NH:26][C:2]1[C:10]2[NH:9][C:8]([C:11]([F:14])([F:13])[F:12])=[N:7][C:6]=2[C:5]([N+:15]([O-:17])=[O:16])=[CH:4][C:3]=1[C:18]#[N:19])[CH3:21]

Participants

3

Reactant 2

HCID 21558567HCID 21558567, compoundHCID 135783926HCID 135783926, compound

Product 1

HCID 135783924HCID 135783924, compound

Procedure

4-Chloro-7-nitro-5-cyano-2-trifluoromethylbenzimidazole is reacted with 2-ethylcyclobutylamine to obtain 4-((2-ethylcyclobutyl)amino)-7-nitro-5-cyano-2-trifluoromethylbenzimidazole, m.w., 353.3.

Sources & evidence

ORD record
ord-10342660990749319bcd3e1dc6da544c
Source dataset
uspto-grants-1976_02
Patent number
US03939166

Reaction notes

Loading…