Acrolein → HCID 10471014, compound

HRID 1415739Notes

Reaction equation

HRID 1415739 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([NH:11][C:12]2[CH:17]=[CH:16][C:15]([S:18](=[O:21])(=[O:20])[NH2:19])=[CH:14][CH:13]=2)[C:9]#N)=[CH:4][CH:3]=1.[CH:22]([CH:24]=C)=O>>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:11]([C:12]3[CH:17]=[CH:16][C:15]([S:18](=[O:21])(=[O:20])[NH2:19])=[CH:14][CH:13]=3)[CH:22]=[CH:24][CH:9]=2)=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 7847AcroleinHCID 21862745HCID 21862745, compound

Product 1

HCID 10471014HCID 10471014, compound

Procedure

Following a procedure similar to that described in Example 1(iii), but using α-(4-fluorophenyl)-α-(4-sulfamoylanilino)acetonitrile [prepared as described in step (ii) above] and acrolein as starting materials, the title compound was obtained as a brown powder (yield 11%), melting at 198-199° C.

Sources & evidence

ORD record
ord-45daf89bc3e648c9bfb0fafbe41a5e93
Source dataset
uspto-grants-1999_06
Patent number
US05908858

Reaction notes

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