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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339314생성일: 2026년 10월 26일

Tris(hydroxymethyl)aminomethane → N-(2,3-dimethylcyclohexyl)benzo[d][1,3]dioxole-5-carboxamide

https://huagongshe.com/reaction/339314

반응식

참여 물질

역할이름HCID투입량
반응물Tris(hydroxymethyl)aminomethaneHCID 6503—
반응물1,3-Benzodioxole-5-carboxylic acidHCID 7196—
반응물2,3-DimethylcyclohexylamineHCID 123507—
반응물CarbodiimideHCID 160435—
반응물HCID 178418300HCID 178418300—
용매DimethylformamideHCID 6228—
용매AcetonitrileHCID 6342—
용매Acetonitrile methylene chlorideHCID 21877088—
생성물N-(2,3-dimethylcyclohexyl)benzo[d][1,3]dioxole-5-carboxamideHCID 17479454—

반응 단계

2,3-dimethylcyclohexanamine (20 μmol) and benzo[d][1,3]dioxole-5-carboxylic acid (1.1 eq) were each dissolved in acetonitrile/dichloromethane (200 μL, 2:1). PS-Carbodiimide resin (2 eq) was loaded into a 1.2 mL 96 well Greiner plate, followed by the addition of amine and acid solutions. Hydroxybenzotriazole (1.1 eq) was dissolved in DMF (100 mL) and was added into the reaction well. The reaction was shaken overnight at room temperature. Once the reaction was completed, PS-Trisamine resin (1.5 eq) was added into the reaction mixture and the solution was allowed to shake overnight at room temperature. Acetonitrile (200 mL) was added into the reaction well, and the top clear solution was transferred into a new plate. The solution was evaporated to give N-(2,3-dimethylcyclohexyl)benzo[d][1,3]dioxole-5-carboxamide. MS (M+H, 276.20).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895050B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-214d46e93fd848efac87ce532459a3b5
출처 메모uspto-grants-2014_11