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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2070260생성일: 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/2070260

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)phenylamino)-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 번호US08299108B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-c37401f37b4f40d3a20d061e078eccf9
출처 메모uspto-grants-2012_10