Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249528Generated: October 30, 2026

1,1-Ethenediamine, N-[(6-chloro-3-pyridinyl)methyl]-N'-methyl-2-nitro- → 1(6-Chloro-3-pyridylmethyl)amino-1-methylamino-2-methanesulfonylthiocarbamoyl-2-nitroethylene

https://huagongshe.com/reaction/249528

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-Ethenediamine, N-[(6-chloro-3-pyridinyl)methyl]-N'-methyl-2-nitro-HCID 4325619—
ReactantMethanesulfonyl isothiocyanateHCID 12297546—
SolventAcetonitrileHCID 6342—
Product1(6-Chloro-3-pyridylmethyl)amino-1-methylamino-2-methanesulfonylthiocarbamoyl-2-nitroethyleneHCID 5989663032.9%

Reaction Steps

In 50 ml of CH3CN was dissolved 0.50 g (0.002 mole) of 1-(6-chloro-3-pyridylmethyl)amino-1-methylamino-2-nitroethylene, followed by addition of 0.30 g (0.002 mole) of methanesulfonyl isothiocyanate. The mixture was stirred at room temperature for 2 hours. The CH3CN was distilled off and the residue was purified by silica gel column chromatography. The procedure gave 0.25 g of the title compound as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05214152
Source datasetuspto-grants-1993_05
ORD IDord-f43c95d859ea4a35b777c0e58f3727a0
Source noteuspto-grants-1993_05