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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012227Generated: October 30, 2026

Hydrochloric Acid → 1-(6-Chloro-3-pyridylmethyl)-3-methyl2-nitroguanidine

https://huagongshe.com/reaction/1012227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
ReactantSodium HydroxideHCID 14798—
Reactant5-(Aminomethyl)-2-chloropyridineHCID 7020927—
Reactant(E)-N-methyl-N'-nitromethoxymethanimidamideHCID 136414659—
SolventWaterHCID 962—
Product1-(6-Chloro-3-pyridylmethyl)-3-methyl2-nitroguanidineHCID 13621819688.9%

Reaction Steps

1.3 g of sodium chloride and 4.65 g of water were mixed, and the resulting mixture was cooled to −10 degree centigrade. N,O-dimethyl-N′-nitroisourea (4.5 g, 0.03 mole) was introduced into the above solution, and 0.58 g (4.64 mmole) of 32% NaOH was further added to the suspension and stirred. Thereafter, [(2-chloro-5-pyridyl)methyl]amine (4.93 g, 0.03 mole) was introduced dropwise to the suspension. Sodium chloride was dissolved in water with 78% of the saturated solubility at a water temperature of −10 degree centigrade. The solution was stirred at −10 degree centigrade for 4 hours and then heated to 20 degree centigrade, and further stirred for 6 hours. Then, 35% hydrochloric acid (0.7 g, 6.71 mmole) was added to the suspension so that the pH became not more than 4. The resulting solution was extracted with ethyl acetate and concentrated under a reduced pressure, and then recrystallized. Thus, 6.5 g of a 1-[(2-chloro-5-pyridyl)methyl]-3-methyl-2-nitroguanidine was obtained. The isolated yield at this time was 81%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977496B2
Source datasetuspto-grants-2011_07
ORD IDord-92a3d774019c4b4781bba48825b47577
Source noteuspto-grants-2011_07