HCID 18313592, compound → HCID 9927612, compound

HRID 277093Notes

Reaction equation

HRID 277093 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.[CH2:21]([C:25]1[CH:26]=[CH:27][C:28](/[CH:31]=[CH:32]/[C:33]#[N:34])=[N:29][CH:30]=1)[CH2:22][CH2:23][CH3:24]>>[CH2:21]([C:25]1[CH:26]=[CH:27][C:28]([C:31]2[CH:32]=[C:33]([NH2:34])[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)=[N:29][CH:30]=1)[CH2:22][CH2:23][CH3:24]

Participants

3

Reactant 2

HCID 18313592HCID 18313592, compoundHCID 178527402HCID 178527402, compound

Product 1

HCID 9927612HCID 9927612, compound

Procedure

The title compound, MS m/e (%): 334 (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 (E)-3-(5-butyl-pyridin-2-yl)-acrylonitrile.

Sources & evidence

ORD record
ord-ce0ac87097854e98b1d95adb70215a1a
Source dataset
uspto-grants-2002_03
Patent number
US06355653B1

Reaction notes

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