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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4365Generated: October 28, 2026

Water → N-[[(4-fluorophenyl)carbamoyl]amino]-1,2,3,6-tetrahydropyridine

https://huagongshe.com/reaction/4365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantN-[[(4-fluorophenyl)carbamoyl]-imino]pyridiniumHCID 20152379—
SolventEthanolHCID 702—
ProductN-[[(4-fluorophenyl)carbamoyl]amino]-1,2,3,6-tetrahydropyridineHCID 13534699—

Reaction Steps

A suspension of N-[[(4-fluorophenyl)carbamoyl]-imino]pyridinium ylide (1.04 g) and sodium borohydride (2.55 g) in ethanol (100 ml) was stirred at ambient temperature for 16 hours. Excess of sodium borohydride was decomposed with water, and the resulting mixture was evaporated. The residue was extracted with chloroform (20 ml×3). The combined organic extract was washed with water, dried over magnesium sulfate and evaporated to give crystalls. Recrystallization from diisopropyl ether gave N-[[(4-fluorophenyl)-carbamoyl]amino]-1,2,3,6-tetrahydropyridine (0.60 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04725608
Source datasetuspto-grants-1988_02
ORD IDord-ba8e9518e9a14e998c41606e7292d98b
Source noteuspto-grants-1988_02