HCID 18313649, compound → HCID 9861971, compound

HRID 277118Notes

Reaction equation

HRID 277118 reaction equation
C1(S([CH2:10][C:11]2[N:12]=[C:13]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=3)[NH:14][N:15]=2)(=O)=O)C=CC=CC=1.[Cl:22][C:23]1[N:28]=[C:27](/[CH:29]=[CH:30]/[C:31]#[N:32])[CH:26]=[CH:25][CH:24]=1>>[Cl:22][C:23]1[N:28]=[C:27]([C:29]2[CH:30]=[C:31]([NH2:32])[N:15]3[N:14]=[C:13]([C:16]4[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=4)[N:12]=[C:11]3[CH:10]=2)[CH:26]=[CH:25][CH:24]=1

Participants

3

Reactant 2

HCID 18313649HCID 18313649, compoundHCID 178527399HCID 178527399, compound

Product 1

HCID 9861971HCID 9861971, compound

Procedure

The title compound, MS m/e (%):323 (M+H+,100), was prepared in accordance with the general method of example 1 from 2-(5-benzenesulfonylmethyl-2H-[1,2,4]triazol-3-yl)-pyridine and E-3-(6-chloro-pyridin-2-yl )-acrylonitrile.

Sources & evidence

ORD record
ord-f24ccc62fdd94b2aa45088f455f4ce14
Source dataset
uspto-grants-2002_03
Patent number
US06355653B1

Reaction notes

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