Furfurylamine → HCID 21392418, compound

HRID 461769Notes

Reaction equation

Br[C:2]1[CH:7]=[C:6]([C:8]([Cl:12])=[C:9]([Cl:11])[Cl:10])[C:5]([S:13]([NH2:16])(=[O:15])=[O:14])=[CH:4][C:3]=1[S:17]([NH2:20])(=[O:19])=[O:18].[CH2:21]([NH2:27])[C:22]1[O:26][CH:25]=[CH:24][CH:23]=1>>[CH2:21]([NH:27][C:2]1[CH:7]=[C:6]([C:8]([Cl:12])=[C:9]([Cl:11])[Cl:10])[C:5]([S:13]([NH2:16])(=[O:15])=[O:14])=[CH:4][C:3]=1[S:17]([NH2:20])(=[O:19])=[O:18])[C:22]1[O:26][CH:25]=[CH:24][CH:23]=1

Participants

Reactant 2

HCID 3438Furfurylamine

HCID 213924354-Bromo-6-trichlorovinyl-1,3-benzenedisulfonamide

Product 1

HCID 21392418HCID 21392418, compound

Procedure

4-Bromo-6-trichlorovinyl-1,3-benzenedisulfonamide and furfurylamine are reacted at 70° C. for 10 hours in analogy to above procedure to give 4-furfurylamino-6-(1,2,2-trichlorovinyl)-1,3-benzenedisulfonamide with m.p. 155°-155° C.

Sources & evidence

ORD record: ord-e682378b472b40fbaa0d7ca666e99ec2
Source dataset: uspto-grants-1977_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04064239

Reaction notes

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