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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6253Generated: October 26, 2026

Triethylamine → 6-Benzyloxyamino-4-chloro-2,5-diformamidopyrimidine

https://huagongshe.com/reaction/6253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantO-BenzylhydroxylamineHCID 102313—
ReactantN-(4,6-dichloro-2-formamido-pyrimidin-5-yl)formamideHCID 13989892—
Solvent1,4-DioxaneHCID 31275—
Product6-Benzyloxyamino-4-chloro-2,5-diformamidopyrimidineHCID 1452396046.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4,6-dichloro-2,5-diformamido-pyrimidine (1.9 g, 8.09 mmol), benzyloxyamine (1 g, 8.13 mmol), triethylamine (2 ml) and dioxan (20 ml) was stirred at 100° C. for 1 hour. The cooled reaction mixture was filtered and the precipitate collected and washed with dioxan (2×5 ml). The filtrate and washings were combined and evaporated to a syrup. Column chromatography on silica gel (eluted with chloroform-ethanol, 30:1) afforded the title compound (1.2 g, 46%). IR: νmax (KBr) 3242, 1694, 1588, 1472 cm-1 ; 1H NMR δH [(CD3)2SO], 4.89 (2H, s, OCH2Ph), 7.4 (5H, m, Ph), 8.15 (1H, s, CHO), 9.18, 9.42 (1H, 2×br.s, D2O exchangeable, NH), 9.25 (1H, br.s, CHO), 10.91 (2H, br.s, D2O exchangeable, 2×NH). m/z (FAB+ve ion, thioglycerol) MH+ 322.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05247085
Source datasetuspto-grants-1993_09
ORD IDord-44cf70cb0643481db455beee7bccf37f
Source noteuspto-grants-1993_09