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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1271027생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1271027

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물N,N-bis(1-methylethyl)formamideHCID 75912—
반응물HCID 178508432HCID 178508432—
용매DichloromethaneHCID 6344—
생성물4-Chloro-2-diisopropylaminomethyleneamino-5-iodopyrimidineHCID 73446451—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07205297B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-2f63d07cd13644f8b01ad385cdc396fe
출처 메모uspto-grants-2007_04