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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2109989생성일: 2026년 10월 25일

Methanol → (1H-benzimidazol-2-yl)-[1-(1-methyl-1H-indol-2-ylmethyl)-piperidin-4-ylmethyl]-amine

https://huagongshe.com/reaction/2109989

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물1-Methylindole-2-carboxaldehydeHCID 267164—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물HCID 11481631HCID 11481631—
용매acetic acid N,N-dimethylformamideHCID 21926011—
생성물(1H-benzimidazol-2-yl)-[1-(1-methyl-1H-indol-2-ylmethyl)-piperidin-4-ylmethyl]-amineHCID 10150398—

반응 단계

After adding 1-methyl-1H-indole-2-carboaldehyde (0.26 mmol) and sodium triacetoxyborohydride (0.26 mmol) to a solution of (1H-benzimidazol-2-yl)-piperidin-4-ylmethyl-amine (20.0 mg, 0.09 mmol) in dimethylformamide-acetic acid (10:1) (1.0 ml), the mixture was stirred at room temperature overnight. Methanol (1.0 ml) was added to the reaction mixture to suspend the reaction, and after stirring for 1 hour, the solution was passed through SCX (Bond Elute SCX500MG: cationic ion-exchange resin, Varian). The SCX was washed with methanol and then with a mixed solution of chloroform/methanol (1/1), and elution was performed with a 2N ammonia-methanol solution. The solvent was distilled off under reduced pressure to obtain (1H-benzimidazol-2-yl)-[1-(1-methyl-1H-indol-2-ylmethyl)-piperidin-4-ylmethyl]-amine. The compound was identified by LC-MS.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07517875B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-547fd898141640baa970d42228aef397
출처 메모uspto-grants-2009_04