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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1790670생성일: 2026년 10월 27일

1-Pyrrolidineethanamine → 4-(2-{[4-(dimethylamino)phenyl]amino-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-N-(2-pyrrolidinylethyl)carboxamide

https://huagongshe.com/reaction/1790670

반응식

참여 물질

역할이름HCID투입량
반응물1-PyrrolidineethanamineHCID 1344—
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
반응물2-{[4-(Dimethylamino)phenylamino)-1-methylbenzimidazol-5-yloxy)-pyridine-2-carboxylic acidHCID 86617166—
용매TetrahydrofuranHCID 8028—
생성물4-(2-{[4-(dimethylamino)phenyl]amino-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-N-(2-pyrrolidinylethyl)carboxamideHCID 131725834—

반응 단계

To 4-(2-{[4-(dimethylamino)pheylamino)-1-methylbenzimidazol-5-yloxy)-pyridine-2-carboxylic acid (1 eq) in tetrahydrofuran was added 2-pyrrolidinylethylamine (2 eq), HBTU (2 eq) and N,N-diisopropylethylamine (4 eq) and stir at ambient temperature for 16 h. The mixture was then concentrated and partitioned between ethyl acetate and water. The organic layer was concentrated and preparative chromatography yielded [4-(2-{[4-(dimethylamino)phenyl]amino-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-N-(2-pyrrolidinylethyl)carboxamide. MS: MH+=498.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07071216B2
출처 데이터셋uspto-grants-2006_07
ORD IDord-4deca450243547aba33d3679d2121b53
출처 메모uspto-grants-2006_07