Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72463생성일: 2026년 10월 24일
Potassium Carbonate → 2-(3-(3-(4-(Tert-butoxycarbonyl)piperazin-1-yl)phenoxy)azetidin-1-yl)-5-chloronicotinic acid
https://huagongshe.com/ko/reaction/72463
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | tert-Butyl 4-(3-hydroxyphenyl)piperazine-1-carboxylate | HCID 18669061 | — |
| 반응물 | Methyl 5-chloro-2-(3-((methylsulfonyl)oxy)azetidin-1-yl)nicotinate | HCID 86697874 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-(3-(3-(4-(Tert-butoxycarbonyl)piperazin-1-yl)phenoxy)azetidin-1-yl)-5-chloronicotinic acid | HCID 67958153 | — |
반응 단계
To a solution of tert-butyl 4-(3-hydroxyphenyl)piperazine-1-carboxylate (D18) (143.18 mg, 0.514 mmole) in dimethylformamide (2 ml), potassium carbonate (71 mg, 0.514 mmol) and the reaction mixture was heated 2 h at 80° C. methyl 5-chloro-2-(3-((methylsulfonyl)oxy)azetidin-1-yl)nicotinate (D63) (150 mg, 0.467 mmol) in dimethylformamide (2 ml) was added dropwise and the resulting mixture stirred 21 h at 120° C. After cooling at room temperature, 1M NaOH (0.935 ml) was added and the mixture stirred 1 h at 120° C. After cooling the reaction mixture was extracted with diethylether (2×10 ml) and the aqueous was evaporated in vacuo. The residue was purified by SPE-Si cartridge (5 g) eluting with a mixture dichloromethane/methanol from 100/0 to 80/20. Collected fractions, after solvent evaporation afforde the title compound (D110) (155 mg)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08828987B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-cc660e40c4514ed698b84628d03b181e |
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| 출처 메모 | uspto-grants-2014_09 |
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