Reaction equation
CSCCC#N.C1SC(NC(N)=N)=NC=1CS[CH2:18][CH2:19][C:20]([NH:22][S:23]([NH2:26])(=[O:25])=[O:24])=[NH:21]>>[S:23]([NH:22][C:20](=[NH:21])[CH:19]=[CH2:18])(=[O:25])(=[O:24])[NH2:26]Participants
3
Procedure
N-sulfamyl-acrylamidine was prepared by a four-step procedure from 3-(methylthio)-propionitrile, with an extremely low (5.5%) yield in several days. The products of the subsequent steps, including famotidine, were isolated by column chromatography.
Workup
- customyield in several days
- customwere isolated by column chromatography
Sources & evidence
- ORD record
- ord-09fcdf6f02f84672bde87c942a1f3963
- Source dataset
- uspto-grants-1989_05
- Patent number
- US04835281
Linked notes
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