HCID 70088294, compound → HCID 22629664, compound

HRID 277099Notes

Reaction equation

HRID 277099 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.[C:21]([CH:23]=[CH:24][C:25]1[CH:30]=[CH:29][C:28]([S:31]([NH:34][C:35]2[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=2)(=[O:33])=[O:32])=[CH:27][CH:26]=1)#[N:22]>>[NH2:22][C:21]1[N:12]2[N:13]=[C:14]([C:16]3[O:17][CH:18]=[CH:19][CH:20]=3)[N:15]=[C:11]2[CH:10]=[C:24]([C:25]2[CH:26]=[CH:27][C:28]([S:31]([NH:34][C:35]3[CH:36]=[CH:37][CH:38]=[CH:39][CH:40]=3)(=[O:33])=[O:32])=[CH:29][CH:30]=2)[CH:23]=1

Participants

3

Reactant 2

HCID 70088294HCID 70088294, compoundHCID 178527402HCID 178527402, compound

Product 1

HCID 22629664HCID 22629664, compound

Procedure

The title compound, MS m/e (%): 430 (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 4-(2-cyano-vinyl)-N-phenyl-benzenesulfonamide

Sources & evidence

ORD record
ord-62242d34b8e84a20885d8fb5b39fd3c2
Source dataset
uspto-grants-2002_03
Patent number
US06355653B1

Reaction notes

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