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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1262111생성일: 2026년 10월 27일

Diisopropylethylamine → 4-{4-[7-(3-tert-Butylsulfamoyl-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-ylamino]-3-methoxy-phenyl}-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1262111

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물N-Propyl-Methyl Piperidinium Bis(trifluoroMethylsulfonyl)ImideHCID 4176748—
반응물Tert-butyl 4-(4-amino-3-methoxyphenyl)piperidine-1-carboxylateHCID 57416157—
반응물HCID 178449976HCID 178449976—
용매DimethylformamideHCID 6228—
생성물4-{4-[7-(3-tert-Butylsulfamoyl-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-ylamino]-3-methoxy-phenyl}-piperidine-1-carboxylic acid tert-butyl esterHCID 66712008—

반응 단계

In a 10 mL sealed tube, to N-tert-Butyl-3-(2-hydroxy-pyrrolo[2,1-f][1,2,4]triazin-7-yl)-benzenesulfonamide (120 mg, 0.3464 mmol) and N,N-Diisopropylethylamine (0.242 mL, 1.39 mmol) in 3.0 mL of anhydrous DMF was added N-Phenylbis(trifluoromethane-sulfonimide (136 mg, 0.381 mmol). After stirring at room temperature for 30 minutes, 4-(4-Amino-3-methoxy-phenyl)-piperidine-1-carboxylic acid tert-butyl ester (140 mg, 0.460 mmol) was added. The reaction mixture was heated at 65° C. for 2.5 days. The reaction mixture was purified via silica gel column chromatography using 100:1 DCM:MeOH as the eluant. The collected fractions afforded impure 4-{4-[7-(3-tert-Butylsulfamoyl-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-ylamino]-3-methoxy-phenyl}-piperidine-1-carboxylic acid tert-butyl ester as a sticky brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08471005B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-c00a0809f58a48fb81cc5b8d8b7d9c38
출처 메모uspto-grants-2013_06