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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1640287생성일: 2026년 10월 26일

N-Ethylbenzylamine → N-benzyl-N-ethyl-6-(2'-oxo-1,1',2',3-tetrahydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-5-yl-amino)pyrimidine-4-carboxamide

https://huagongshe.com/reaction/1640287

반응식

참여 물질

역할이름HCID투입량
반응물N-EthylbenzylamineHCID 84352—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물6-(2'-Oxo-1,1',2',3-tetrahydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-5-yl-amino)pyrimidine-4-carboxylic acid-hydrochlorideHCID 66722185—
용매DimethylformamideHCID 6228—
생성물N-benzyl-N-ethyl-6-(2'-oxo-1,1',2',3-tetrahydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-5-yl-amino)pyrimidine-4-carboxamideHCID 49801374—

반응 단계

100 mg (0.24 mmol) 6-(2′-oxo-1,1′,2′,3-tetrahydrospiro[indene-2,3′-pyrrolo[2,3-b]pyridin]-5-ylamino)pyrimidine-4-carboxylic acid hydrochloride, 50 μL (0.33 mmol) benzyl-ethyl-amine, 0.10 mL (0.72 mmol) TEA and 85 mg (0.27 mmol) TBTU in 1.8 mL DMF were stirred overnight at RT. The purification was carried out by preparative HPLC-MS. The product-containing fractions were combined and lyophilised.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08110575B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-6564e9956e884df2ad29614950053b8c
출처 메모uspto-grants-2012_02