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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1678055생성일: 2026년 10월 26일

Ethyl-oxido-oxo-sulfanylidene-lambda6-sulfane → 4-Chloro-5-methylthiothieno[2,3-d]pyrimidine

https://huagongshe.com/reaction/1678055

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl-oxido-oxo-sulfanylidene-lambda6-sulfaneHCID 3633702—
반응물5-Bromo-4-chlorothieno[2,3-d]pyrimidineHCID 45480299—
반응물HCID 178418918HCID 178418918—
용매TetrahydrofuranHCID 8028—
생성물4-Chloro-5-methylthiothieno[2,3-d]pyrimidineHCID 87350514127.7%

반응 조건

온도0 °C

반응 단계

5-bromo-4-chlorothieno[2,3-d]pyrimidine (750 mg, 3.0 mmol) was partially dissolved in anh. THF (8 mL), cooled to 0° C. and treated in portions with a 2M THF solution of i-PrMgCl (2.0 mL, 4.0 mmol). After 20 minutes, this solution was treated dropwise with methylmethanethiosulfonate (460 μl, 570 mg, 4.5 mmol). The cooling bath was removed and the mixture was stirred for 4 hours at 25° C. The reaction was quenched with saturated aqueous NH4Cl and extracted with EtOAc. The organic phase was washed with water, brine, dried (Na2SO4) and evaporated to give 830 mg crude product-ca 80 percent pure by GC. The material was purified by recrystallization from hot heptane to give 350 mg (45 percent) yield of tan crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08008487B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-35b841885da84ec48b95de1638c53f9d
출처 메모uspto-grants-2011_08