Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70883생성일: 2026년 10월 23일
Sodium Carbonate → (R)-ethyl 3-(tert-butoxycarbonylamino)-4-(2',5'-dichlorobiphenyl-4-yl)butanoate
https://huagongshe.com/ko/reaction/70883
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | 2,5-Dichlorobenzeneboronic acid | HCID 2773371 | — |
| 반응물 | (R)-Ethyl 4-(4-bromophenyl)-3-((tert-butoxycarbonyl)amino)butanoate | HCID 59607624 | — |
| 촉매 | HCID 178418397 | HCID 178418397 | — |
| 용매 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 용매 | Sodium chloride; water | HCID 57417360 | — |
| 생성물 | (R)-ethyl 3-(tert-butoxycarbonylamino)-4-(2',5'-dichlorobiphenyl-4-yl)butanoate | HCID 59607666 | 92.7% |
반응 단계
A mixture of (R)-ethyl 4-(4-bromophenyl)-3-(tert-butoxycarbonylamino)butanoate (1.005 g, 2.60 mmol), 2,5-dichlorophenylboronic acid (0.745 g, 3.90 mmol), Pd(PPh3)4 (0.301 g, 0.260 mmol) and 2 M aqueous Na2CO3 (2.60 ml, 5.20 mmol) in 1,2-dimethoxyethane (20 ml) is allowed to stir at 95° C. under nitrogen for 3 hours. The reaction mixture is cooled to room temperature and diluted with brine. The two phases are separated. The products are extracted twice with ethyl acetate (2×100 ml) from the aqueous layer. The combined organic layer is washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure. The obtained residue is purified by silica gel flash column chromatography (heptane/EtOAc=100:0 to 70:30) to give (R)-ethyl 3-(tert-butoxycarbonylamino)-4-(2′,5′-dichlorobiphenyl-4-yl)butanoate (1.09 g); HPLC retention time=1.50 minutes (condition B); MS (ES+)=352.00 (m-BOC+2; 100%); 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.28 (t, J=7.1 Hz, 3 H) 1.41 (s, 9 H) 2.45-2.58 (m, 2 H) 2.85-3.00 (m, 2 H) 4.17 (t, J=7.1 Hz, 2 H) 4.20 (br s, 1 H) 5.06-5.08 (m, 1 H) 7.23-7.28 (m, 3 H) 7.31-7.40 (m, 4 H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08822534B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-6096ed87b8c84fda8d76fb191abd16d1 |
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| 출처 메모 | uspto-grants-2014_09 |
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