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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271027Generated: October 25, 2026

Oxalyl chloride → 4-Chloro-2-diisopropylaminomethyleneamino-5-iodopyrimidine

https://huagongshe.com/reaction/1271027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantN,N-bis(1-methylethyl)formamideHCID 75912—
ReactantHCID 178508432HCID 178508432—
SolventDichloromethaneHCID 6344—
Product4-Chloro-2-diisopropylaminomethyleneamino-5-iodopyrimidineHCID 73446451—

Reaction Steps

A solution of 4.5 mL of oxalyl chloride in 35 mL of dichloromethane was added dropwise over 25 minutes to an ice water bath-cooled solution of 7.0 mL of N,N-diisopropylformamide in 65 mL of dichloromethane with magnetic stirring. After a few minutes, 4.74 g of 2-amino-4-hydroxy-5-iodopyrimidine was added in one portion. The bath was removed and the solution was stirred at room temperature for 30 minutes, then refluxed for one and one half hours. The solution was cooled and poured into an equal amount of ice-cold saturated aqueous sodium bicarbonate with stirring. The two phases were partitioned and the organic layer washed with additional bicarbonate(2×), water(1×) and finally saturated aqueous brine. After drying over sodium sulfate and filtration, the solution was evaporated in vacuo to yield 10.13 g of a reddish oil. The oil was purified by column chromatography on silica gel, eluting with dichloromethane. Like fractions were pooled, evaporated and triturated with hexanes to give white free flowing crystals, 5.94 g, m.p. 97–100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205297B2
Source datasetuspto-grants-2007_04
ORD IDord-2f63d07cd13644f8b01ad385cdc396fe
Source noteuspto-grants-2007_04