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HRID 1678055作成日:2026年10月26日

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

https://huagongshe.com/reaction/1678055

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl-oxido-oxo-sulfanylidene-lambda6-sulfaneHCID 3633702—
反応物5-Bromo-4-chlorothieno[2,3-d]pyrimidineHCID 45480299—
反応物HCID 178418918HCID 178418918—
溶媒TetrahydrofuranHCID 8028—
生成物4-Chloro-5-methylthiothieno[2,3-d]pyrimidineHCID 87350514127.7%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08008487B2
出典データセットuspto-grants-2011_08
ORD IDord-35b841885da84ec48b95de1638c53f9d
出典メモuspto-grants-2011_08