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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1096871생성일: 2026년 10월 26일

Tributylphosphine → 6-[Cyclopropyl-(3-methoxy-2-methylbenzyl)carbamoyl]-7-{2-[2-(2,6-dichloro-4-methylphenoxy)ethoxy]thiazol-5-yl}-3,9-diazabicyclo[3.3.1]non-6-ene-3,9-dicarboxylic acid di-tert-butyl ester

https://huagongshe.com/reaction/1096871

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참여 물질

역할이름HCID투입량
반응물TributylphosphineHCID 13831—
반응물2,6-Dichloro-4-methylphenolHCID 17077—
반응물6-[Cyclopropyl-(3-methoxy-2-methylbenzyl)carbamoyl]-7-[2-(2-hydroxyethoxy)thiazol-5-yl]-3,9-diazabicyclo[3.3.1]non-6-ene-3,9-dicarboxylic acid di-tert-butyl esterHCID 68570797—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
생성물6-[Cyclopropyl-(3-methoxy-2-methylbenzyl)carbamoyl]-7-{2-[2-(2,6-dichloro-4-methylphenoxy)ethoxy]thiazol-5-yl}-3,9-diazabicyclo[3.3.1]non-6-ene-3,9-dicarboxylic acid di-tert-butyl esterHCID 6857106576%

반응 조건

온도80 °C

반응 단계

A sol. of 2,6-dichloro-p-cresol (0.55 mmol; 97 mg) in toluene (4.8 mL) was treated with compound E9 (0.37 mmol; 250 mg) followed by azodicarboxylic dipiperidide (0.73 mmol; 184 mg) and PBu3 (1.28 mmol; 0.27 mL). The reaction mixture was stirred at 80° C. After 1 h, the reaction mixture was allowed to cool to rt, diluted with Et2O (50 mL), filtrated, and the filtrate was washed with NaOH 1M (50 mL) and brine (50 mL). The org. extract was dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (EtOAc/heptane 30:70) yielded the title compound (0.23 g, 76%). LC-MS: tR=1.25 min; ES+: 843.29.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08138340B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-8113673050884606b0e167c280617300
출처 메모uspto-grants-2012_03