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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131205생성일: 2026년 10월 26일

Triethylamine → 4-[4-Nitro-3-(2-phenoxy-acetylamino)-phenyl]-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/131205

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Phenoxyacetyl chlorideHCID 69703—
반응물Tert-butyl 4-(3-amino-4-nitrophenyl)piperazine-1-carboxylateHCID 22272542—
용매TetrahydrofuranHCID 8028—
생성물4-[4-Nitro-3-(2-phenoxy-acetylamino)-phenyl]-piperazine-1-carboxylic acid tert-butyl esterHCID 6846364381.3%

반응 단계

A mixture of 1 g (3.1 mmol) 4-(3-amino-4-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester, 0.793 g (4.65 mmol) phenoxyacetyl chloride and 2.2 g (21.7 mmol) triethylamine in 20 ml THF was stirred at room temperature for 30 min. The mixture was evaporated and 100 ml DCM were added. The organic phase was washed with 2×50 ml 0.1 M Na2CO3 aq. The combined aqueous phase was extracted with 2×100 ml DCM. The combined organic phases were dried with MgSO4 and evaporated to dryness. The residue was purified over silica eluting with ethyl acetate/hexane 1/1 to yield 1.15 g (81%) of the title compound as yellow solid. MS(ISP): 455.3 (M−H)−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384945B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-bd6f8070862c4cd49214fc4ab082ceaa
출처 메모uspto-grants-2008_06