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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1005653생성일: 2026년 10월 26일

Pyrrolidine → tert-butyl 4-(1H-indol-7-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1005653

반응식

참여 물질

역할이름HCID투입량
반응물PyrrolidineHCID 31268—
반응물Dimethylformamide dimethyl acetalHCID 78373—
반응물4-(3-Methyl-2-nitrophenyl)-piperazine-1-carboxylic acid tert-butyl esterHCID 60108775—
용매DimethylformamideHCID 6228—
생성물tert-butyl 4-(1H-indol-7-yl)piperazine-1-carboxylateHCID 2107095126.8%

반응 단계

A solution of 4-(3-methyl-2-nitrophenyl)-piperazine-1-carboxylic acid tert-butyl ester (10 g, 31 mmol), N,N-dimethylformamide dimethyl acetal (13.2 mL, 100 mmol) and pyrrolidine (4 mL, 50 mmol) in 45 mL of DMF was heated under reflux for 20 h. The mixture was concentrated in vacuo and the residue was partitioned between ethyl acetate and water. The ethyl acetate was dried and evaporated. The residue was hydrogenated in 200 mL of THF containing 2.5 g of 10% Pd-C at 50 psi for 6 h. The mixture was filtered, concentrated in vacuo, and partitioned between ethyl acetate and aqueous HCl. The ethyl acetate was washed with brine, dried and evaporated. Silica gel chromatography (10% ethyl acetate-hexane) afforded 2.5 g of 4-(1H-Indol-7-yl)-piperazine-1-carboxylic acid tert-butyl ester (19) as a white solid, m.p. 150-151° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06787535B2
출처 데이터셋uspto-grants-2004_09
ORD IDord-159b9b19f9c24f1eb3a2e5b4c77702d4
출처 메모uspto-grants-2004_09