Methacrolein → HCID 9905955, compound

HRID 1415818Notes

Reaction equation

HRID 1415818 reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]([CH:9]([NH:12][C:13]2[CH:18]=[CH:17][C:16]([S:19](=[O:22])(=[O:21])[NH2:20])=[CH:15][CH:14]=2)[C:10]#N)[CH:5]=[CH:6][C:7]=1[CH3:8].O=[CH:24][C:25](=C)[CH3:26]>>[CH3:26][C:25]1[CH:10]=[C:9]([C:4]2[CH:5]=[CH:6][C:7]([CH3:8])=[C:2]([CH3:1])[CH:3]=2)[N:12]([C:13]2[CH:18]=[CH:17][C:16]([S:19](=[O:22])(=[O:21])[NH2:20])=[CH:15][CH:14]=2)[CH:24]=1

Participants

3

Reactant 2

HCID 6562MethacroleinHCID 21862877alpha-(3,4-Dimethylphenyl)-alpha-(4-sulfamoylanilino)acetonitrile

Product 1

HCID 9905955HCID 9905955, compound

Procedure

Following a procedure similar to that described in Example 1(iii), but using α-(3,4-dimethylphenyl)-α-(4-sulfamoylanilino)acetonitrile [prepared as described in step (ii) above] and methacrolein as starting materials, the title compound was obtained as a slightly brown amorphous powder (yield 69%).

Sources & evidence

ORD record
ord-0e1517d2d2f84ce580f3cda17593e6ad
Source dataset
uspto-grants-1999_06
Patent number
US05908858

Reaction notes

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