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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1986191생성일: 2026년 10월 24일

Sodium Carbonate → [2-(2-Chloropyrimidin-4-yl)-benzo[b]thiophen-6-ylmethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/1986191

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물Triisopropyl borateHCID 21531—
반응물2,4-DichloropyrimidineHCID 77531—
반응물Lithium diisopropylamineHCID 45051747—
반응물HCID 68856189HCID 68856189—
촉매palladium(II) acetateHCID 167845—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물[2-(2-Chloropyrimidin-4-yl)-benzo[b]thiophen-6-ylmethyl]-carbamic acid tert-butyl esterHCID 8662534828.3%

반응 조건

온도-78 °C

반응 단계

Benzo[b]thiophen-6-ylmethyl-carbamic acid tert-butyl ester (3.6 g, 13.8 mmol) is dissolved in THF (100 mL) and cooled to −78° C. Triisopropylborate (8.5 mL) is added, followed by lithium diisopropylamine solution (27 mL of 2.0 M solution), and the reaction is allowed to slowly warm to room temperature over two hours. The reaction is stirred at room temperature for two hours at which time 2,4-dichloropyrimidine (4.59 g, 30.8 mmol), 1,1′-bis(diphenylphosphino)ferrocene (388 mg, 0.700 mmol), palladium (II) acetate (164 mg, 0.730 mmol) and sodium carbonate (28 mL of 2.0 N solution) are added. The reaction is heated for 20 hours at 70° C. After the reaction solution is cooled to 25° C., water (100 mL) is added. The mixture is extracted with dichloromethane and the extracts are evaporated. The resulting solid is subjected to chromatography on silica gel, eluting with EtOAc/hexanes 5-50%, to give the title compound (1.47 g, 28% yield). ES+(m/z) 376 (35Cl) and 378 (37Cl) [M+H].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07547691B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-e08a8a8ea1ef49318e0c9e06e6350068
출처 메모uspto-grants-2009_06