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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | (3-Bromophenyl)boronic acid | HCID 2734318 | — |
| 반응물 | (S)-2-(2-bromo-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyethyl pivalate | HCID 86699799 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | (S)-2-(2-(3-bromophenyl)-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyethanol | HCID 86699802 | 36% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09096586B2 |
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| 출처 데이터셋 | uspto-grants-2015_08 |
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| ORD ID | ord-b426f5bb481c4ebf85868b1de9b05207 |
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| 출처 메모 | uspto-grants-2015_08 |
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