HCID 70090133, compound → HCID 9796582, compound

HRID 277098Notes

Reaction equation

HRID 277098 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.[CH3:21][O:22][C:23]1[N:28]=[C:27](C=CC#N)[CH:26]=[CH:25][CH:24]=1>>[O:17]1[CH:18]=[CH:19][CH:20]=[C:16]1[C:14]1[N:15]=[C:11]2[CH:10]=[C:20]([C:26]3[CH:27]=[N:28][C:23]([O:22][CH3:21])=[CH:24][CH:25]=3)[CH:16]=[C:14]([NH2:13])[N:12]2[N:13]=1

Participants

3

Reactant 2

HCID 70090133HCID 70090133, compoundHCID 178527402HCID 178527402, compound

Product 1

HCID 9796582HCID 9796582, compound

Procedure

The title compound, MS m/e (%): 307 (M+, 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-(6-methoxy-pyridin-2-yl)-acrylonitrile.

Sources & evidence

ORD record
ord-9d69fb5f7a2947208903f2faaa3d859a
Source dataset
uspto-grants-2002_03
Patent number
US06355653B1

Reaction notes

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