Picolyl chloride hydrochloride → N-Cyano-N'-(2-propyn-1-yl)-N"-{2-[(2-pyridyl)methylthio]ethyl}guanidine
Reaction equation
[C:1]([NH:3][C:4]([NH:9][CH2:10][C:11]#[CH:12])=[N:5][CH2:6][CH2:7][SH:8])#[N:2].Cl.Cl[CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=1>>[C:1]([NH:3][C:4]([NH:9][CH2:10][C:11]#[CH:12])=[N:5][CH2:6][CH2:7][S:8][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=1)#[N:2]Participants
3
Procedure
The ethanolic solution of the product of Step A is reacted with about an equimolar amount of 2-chloromethylpyridine hydrochloride and about two equivalents of base to produce the title product.
Sources & evidence
- ORD record
- ord-cb3872faaca34f5f8184fdfb757467e3
- Source dataset
- uspto-grants-1981_08
- Patent number
- US04282363
Reaction notes
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