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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 510271생성일: 2026년 10월 27일

Methanol → (S)-2-(2-(3-bromophenyl)-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyethanol

https://huagongshe.com/reaction/510271

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Sodium HydroxideHCID 14798—
반응물(3-Bromophenyl)boronic acidHCID 2734318—
반응물(S)-2-(2-bromo-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyethyl pivalateHCID 86699799—
용매1,4-DioxaneHCID 31275—
생성물(S)-2-(2-(3-bromophenyl)-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyethanolHCID 8669980236%

반응 조건

온도90 °C

반응 단계

To a solution of (S)-2-(2-bromo-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyethyl pivalate (310 mg, 0.577 mmol) in dioxane (5 mL), was added 3-bromophenylboronic acid (173 mg, 0.865 mmol), Ph(PPh3)4 (33 mg, 0.029 mmol) 2N K2CO3 (850 μL) in sealed tube. The reaction mixture was heated at 90° C. for 3 hs. Then the reaction was cooled down and to the mixture was added MeOH (5 mL), 2N NaOH (1.5 mL) and heated at 45° C. After the reaction was finished, the reaction was washed by water, extracted by EtOAc. The organic phase was dried over MgSO4, filtered, concentrated down and purified by silica gel column, eluting by 0-50% EtOAc in hexanes to give the product (110 mg, 36%). LCMS-ESI+: calc'd for C26H25BrClNO2S: 530.0 (M+H+); Found: 530.2 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09096586B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-b426f5bb481c4ebf85868b1de9b05207
출처 메모uspto-grants-2015_08