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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 909235생성일: 2026년 10월 27일

(3-tert-Butyl-isoxazol-5-yl)-carbamic acid 4-nitrophenyl ester → 4-[2-(5-{2-[3-(3-tert-Butyl-isoxazol-5-yl)-ureidomethyl]-4-fluorophenoxy}-indazol-1-yl)-ethyl]-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/909235

반응식

참여 물질

역할이름HCID투입량
반응물(3-tert-Butyl-isoxazol-5-yl)-carbamic acid 4-nitrophenyl esterHCID 67408902—
반응물4-{2-[5-(2-Aminomethyl-4-fluorophenoxy)-indazol-1-yl]-ethyl}-piperazine-1-carboxylic acid tert-butyl esterHCID 67411679—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물4-[2-(5-{2-[3-(3-tert-Butyl-isoxazol-5-yl)-ureidomethyl]-4-fluorophenoxy}-indazol-1-yl)-ethyl]-piperazine-1-carboxylic acid tert-butyl esterHCID 6740961083%

반응 단계

A solution of 4-{2-[5-(2-aminomethyl-4-fluorophenoxy)-indazol-1-yl]-ethyl}-piperazine-1-carboxylic acid tert-butyl ester (0.050 g, 0.107 mmol) dissolved in dichloromethane (2 mL) was treated with (3-tert-butyl-isoxazol-5-yl)-carbamic acid 4-nitrophenyl ester (0.081 g, 0.266 mmol) and stirred at room temperature for 24 hours. The mixture was diluted with ethyl acetate (60 mL), washed with 1N NaOH (5 mL), water (2×10 mL), brine, dried over MgSO4, and concentrated under reduced pressure. The residue was chromatographed eluting with acetone/hexanes (2:3, then 1:1) to afford 0.056 g of product (83% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08017641B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-c9df2679533e49c694e0e0a072b230cc
출처 메모uspto-grants-2011_09