Methylamine → HCID 59896620, compound
Reaction equation
[Cl:1][C:2]1[N:7]=[CH:6][C:5]([CH2:8][NH:9][C:10](SC)=[CH:11][N+:12]([O-:14])=[O:13])=[CH:4][CH:3]=1.O.[NH2:18][NH2:19].CSC(NCC1C=NC=CC=1)=C[N+]([O-])=O.CN>>[Cl:1][C:2]1[N:7]=[CH:6][C:5]([CH2:8][NH:9][C:10]([NH:18][NH2:19])=[CH:11][N+:12]([O-:14])=[O:13])=[CH:4][CH:3]=1Participants
5
Procedure
The reaction procedure of Example 3 was repeated except that 1-(6-chloro-3pyridylmethyl)amino-1-methylthio-2-nitroethylene and hydrazine hydrate were used in lieu of 1-methylthio-1-(3-pyridylmethyl)amino-2-nitroethylene and aqueous methylamine solution, respectively. The procedure gave the title compound as pale yellow crystals.
Workup
- customThe reaction procedure of Example 3
Sources & evidence
- ORD record
- ord-13269a2322b64f2c9983d5061198c84f
- Source dataset
- uspto-grants-1992_12
- Patent number
- US05175301
Reaction notes
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