HCID 70086894, compound → HCID 18313575, compound

HRID 277095Notes

Reaction equation

HRID 277095 reaction equation
C1(S([CH2:10][C:11]2[N:15]=[C:14]([C:16]3[O:17][CH:18]=[CH:19][CH:20]=3)[NH:13][N:12]=2)(=O)=O)C=CC=CC=1.[F:21][C:22]1[CH:27]=[C:26]([CH:28]=[CH:29][C:30]#[N:31])[CH:25]=[CH:24][N:23]=1>>[F:21][C:22]1[CH:27]=[C:26]([C:28]2[CH:29]=[C:30]([NH2:31])[N:12]3[N:13]=[C:14]([C:16]4[O:17][CH:18]=[CH:19][CH:20]=4)[N:15]=[C:11]3[CH:10]=2)[CH:25]=[CH:24][N:23]=1

Participants

3

Reactant 2

HCID 70086894HCID 70086894, compoundHCID 178527402HCID 178527402, compound

Product 1

HCID 18313575HCID 18313575, compound

Procedure

The title compound, MS m/e (%): 296 (M+H+, 100), was prepared in accordance with the general method of example 1 from 3-benzenesulfonylmethyl-5-furan-2-yl-1H-[1,2,4]triazole and 3-(2-fluoro-pyridin-4-yl)-acrylonitrile.

Sources & evidence

ORD record
ord-0c4b677441f2465eb474e28bae32e392
Source dataset
uspto-grants-2002_03
Patent number
US06355653B1

Reaction notes

Loading…