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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730919Generated: November 2, 2026

3-Pyridinemethanamine → Pyrinuron

https://huagongshe.com/reaction/1730919

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PyridinemethanamineHCID 31018—
ReactantBenzene, 1-isocyanato-4-nitro-HCID 66012—
SolventTolueneHCID 1140—
ProductPyrinuronHCID 4081398%

Reaction Steps

A solution of 415 g. of crude p-nitrophenyl isocyanate in 4.5 l. of toluene was stirred at room temperature. The mixture was filtered and 35 g. of insoluble impurity removed. The material in solution was 380 g. (2.32 mol) of purified p-nitrophenyl isocyanate. The solution was stirred under dry nitrogen, and 3-(aminomethyl)pyridine (250 g., 2.32 mol) was added dropwise. An exotherm to 40° C. was noted. The resulting thick suspension was stirred overnight and then vacuum filtered. The product was washed with hexane and dried in a vacuum oven at 60° C. overnight to give 610.7 g. melting at 220°-221.5° C. The product was a 98% yield of 1-(3-pyridylmethyl)-3-(4-nitrophenyl)urea. This product after recrystallization from 2-methoxyethanol melted with decomposition at 223°-225° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03994905
Source datasetuspto-grants-1976_11
ORD IDord-e28c4fc4d8bb4d3a9593d37a0004b69a
Source noteuspto-grants-1976_11