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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl-oxido-oxo-sulfanylidene-lambda6-sulfane | HCID 3633702 | — |
| 반응물 | 5-Bromo-4-chlorothieno[2,3-d]pyrimidine | HCID 45480299 | — |
| 반응물 | HCID 178418918 | HCID 178418918 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-Chloro-5-methylthiothieno[2,3-d]pyrimidine | HCID 87350514 | 127.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08008487B2 |
|---|
| 출처 데이터셋 | uspto-grants-2011_08 |
|---|
| ORD ID | ord-35b841885da84ec48b95de1638c53f9d |
|---|
| 출처 메모 | uspto-grants-2011_08 |
|---|