Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 388772생성일: 2026년 10월 25일
Dichloromethane → Tert-butyl 2-(4-((2,2-difluorobenzo[d][1,3]dioxole-5-carboxamido)methyl)piperidin-1-yl)ethylcarbamate
https://huagongshe.com/reaction/388772
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dichloromethane | HCID 6344 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 2,2-Difluoro-1,3-benzodioxole-5-carbonyl chloride | HCID 2774064 | — |
| 반응물 | Tert-butyl 2-(4-(aminomethyl)piperidin-1-yl)ethylcarbamate | HCID 57993236 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | Tert-butyl 2-(4-((2,2-difluorobenzo[d][1,3]dioxole-5-carboxamido)methyl)piperidin-1-yl)ethylcarbamate | HCID 57993507 | — |
반응 단계
A solution of tert-butyl 2-(4-(aminomethyl)piperidin-1-yl)ethylcarbamate (50 mg, 0.19 mmol) and TEA (135 μL, 0.972 mmol) in a mixture of 1:1 CH2Cl2:THF (2.5 mL) was treated with 2,2-difluorobenzo[d][1,3]dioxole-5-carbonyl chloride (51 mg, 0.23 mmol). The resulting solution was stirred overnight, then transferred to a test tube containing saturated aqueous NaHCO3 (4 mL) and EtOAc (4 mL). The biphasic mixture was mixed vigorously and allowed to separate for 15 minutes. After separation, the mixture was cooled to −20° C. until the aqueous layer was frozen. The organic layer was then poured off and the solvent was removed under reduced pressure at 50° C. The resulting residue was purified by HiTOPs.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08377968B2 |
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| 출처 데이터셋 | uspto-grants-2013_02 |
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| ORD ID | ord-8939946db5b144559c8d3974fb28389b |
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| 출처 메모 | uspto-grants-2013_02 |
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