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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 966503생성일: 2026년 10월 26일

Potassium Iodide → 2-Methyl-7-pyrrolidin-1-ylmethyl-3,7,8,9-tetrahydro-pyrano[3,2-e]indole-1-carboxylic Acid Benzyl Ester

https://huagongshe.com/reaction/966503

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물PyrrolidineHCID 31268—
반응물Ethyl acetate methanol triethylamineHCID 21980445—
반응물7-Bromomethyl-2-methyl-3,7,8,9-tetrahydro-pyrano[3,2-e]indole-1-carboxylic acid benzyl esterHCID 23393886—
용매AcetonitrileHCID 6342—
생성물2-Methyl-7-pyrrolidin-1-ylmethyl-3,7,8,9-tetrahydro-pyrano[3,2-e]indole-1-carboxylic Acid Benzyl EsterHCID 2339388740%

반응 단계

7-Bromomethyl-2-methyl-3,7,8,9-tetrahydro-pyrano[3,2-e]indole-1-carboxylic acid benzyl ester (0.160 g, 0.390 mmol, 1 eq) was suspended in dry acetonitrile (10 mL) under Ar. Potassium iodide (catalytic) was added followed by the addition of pyrrolidine (0.125 mL, 1.50 mmol, 3.75 eq). The reaction mixture was stirred and heated to reflux. The reaction was followed by TLC (ethyl acetate/methanol/triethylamine 87/10/3). After 18 hours, the reaction was quenched with aqueous sodium bicarbonate and extracted with ethyl acetate (3×). The combined organic extracts were washed with brine and dried over Na2SO4. After removing the solvent, the residue was loaded on silica gel and chromatographed, eluting with ethyl acetate /methanol/triethylamine 87/10/3. 0.063 g (40% yield) of the indole-pyrrolidine was obtained as a white solid. This was converted to the .HCl salt, LC/MS (ESI+) 405 (M+1), Anal. (C25H28N2O3.HCl.0.2 DMF) C, H, N.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06951848B2
출처 데이터셋uspto-grants-2005_10
ORD IDord-5e615d1095cd4124b49f917df5933713
출처 메모uspto-grants-2005_10