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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | N-Propyl-Methyl Piperidinium Bis(trifluoroMethylsulfonyl)Imide | HCID 4176748 | — |
| 반응물 | Tert-butyl 4-(4-amino-3-methoxyphenyl)piperidine-1-carboxylate | HCID 57416157 | — |
| 반응물 | HCID 178449976 | HCID 178449976 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 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 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08471005B2 |
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| 출처 데이터셋 | uspto-grants-2013_06 |
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| ORD ID | ord-c00a0809f58a48fb81cc5b8d8b7d9c38 |
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| 출처 메모 | uspto-grants-2013_06 |
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