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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

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Sodium BicarbonateHCID 516892—
반응물2,2-Difluoro-1,3-benzodioxole-5-carbonyl chlorideHCID 2774064—
반응물Tert-butyl 2-(4-(aminomethyl)piperidin-1-yl)ethylcarbamateHCID 57993236—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Tert-butyl 2-(4-((2,2-difluorobenzo[d][1,3]dioxole-5-carboxamido)methyl)piperidin-1-yl)ethylcarbamateHCID 57993507—

반응 조건

온도-20 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08377968B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-8939946db5b144559c8d3974fb28389b
출처 메모uspto-grants-2013_02