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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77431생성일: 2026년 10월 24일

Triethylamine → 1-Boc-4-(2,3-dihydrobenzo[b][1,4]dioxin-6-ylsulfonyl)piperazine

https://huagongshe.com/ko/reaction/77431

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물2,3-Dihydro-1,4-benzodioxine-6-sulfonyl chlorideHCID 2776169—
용매DichloromethaneHCID 6344—
생성물1-Boc-4-(2,3-dihydrobenzo[b][1,4]dioxin-6-ylsulfonyl)piperazineHCID 46179882100.2%

반응 단계

1-Boc-piperazine (250 mg, 1.34 mmol, 1 equiv.) was dissolved in dichloromethane (2.5 mL) and cooled in an ice bath under nitrogen atmosphere. Triethylamine (375 μl, 2.68 mmol, 2.0 equiv.) was added followed by portionwise addition of 2,3-dihydrobenzo[b][1,4]dioxine-6-sulfonyl chloride (346 mg, 1.48 mmol, 1.1 equiv.). The reaction was stirred in the ice bath for one hour, then quenched with saturated aqueous ammonium chloride (˜3 mL). The organic layer was washed twice with saturated ammonium chloride, once with brine, dried over sodium sulfate and concentrated in vacuo and then purified on silica gel chromatography using a 95/5-5/95, hexane/EtOAc (v/v) gradient to give 1-boc-4-(2,3-dihydrobenzo[b][1,4]dioxin-6-ylsulfonyl)piperazine as a white powder (516 mg, 89% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841305B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-1bdc64ddb3a04ed993f522192a6d5c09
출처 메모uspto-grants-2014_09