Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1986632생성일: 2026년 10월 26일
Potassium Carbonate → (2S,5R)-4-[3-(6-bromo-chroman-3-ylamino)-propyl]-2,5-dimethyl-piperazine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1986632
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 6-Bromochroman-3-amine | HCID 16244432 | — |
| 반응물 | (2S,5R)-4-(3-chloro-propyl)-2,5-dimethyl-piperazine-1-carboxylic acid tert-butyl ester | HCID 57722505 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (2S,5R)-4-[3-(6-bromo-chroman-3-ylamino)-propyl]-2,5-dimethyl-piperazine-1-carboxylic acid tert-butyl ester | HCID 68866043 | 100% |
반응 단계
A mixture of 6-bromo-chroman-3-ylamine (0.105 g, 0.46 mmol, 1 eq), (2S,5R)-4-(3-chloro-propyl)-2,5-dimethyl-piperazine-1-carboxylic acid tert-butyl ester (0.133 g, 0.46 mmol, 1 eq), K2CO3 (0.127 g, 0.92 mmol, 2 eq), and Kl (0.017 g, 0.10 mmol, 0.2 eq) in DMF (0.5 mL) was heated in a microwave reactor at 150° C. for 25 min. The reaction mixture was partitioned between EtOAc (3 mL) and 10% aqueous NaHCO3 (3 mL). The organic layer was separated and aqueous layer was extracted with EtOAc (2 mL×3). The combined organic layers were dried (Na2SO4) and concentrated in vacuo to give 0.22 g (100%) of (2S,5R)-4-[3-(6-bromo-chroman-3-ylamino)-propyl]-2,5-dimethyl-piperazine-1-carboxylic acid tert-butyl ester as a yellow oil. The material was carried on to next step without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07550467B2 |
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| 출처 데이터셋 | uspto-grants-2009_06 |
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| ORD ID | ord-6690ffd8115142f48e3a709399f8d63c |
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| 출처 메모 | uspto-grants-2009_06 |
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