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Dichloromethane → 5-(3-chloropropyl)-2-methyl-5H-furo[3,2-c]pyridin-4-one

HRID 1504222
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HRID 1504222 반응식
CS(Cl)(=O)=O.Cl[CH2:7][Cl:8].OC[CH2:11][CH2:12][N:13]1[CH:18]=[CH:17][C:16]2[O:19][C:20]([CH3:22])=[CH:21][C:15]=2[C:14]1=[O:23]>C(N(CC)CC)C>[Cl:8][CH2:7][CH2:11][CH2:12][N:13]1[CH:18]=[CH:17][C:16]2[O:19][C:20]([CH3:22])=[CH:21][C:15]=2[C:14]1=[O:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6344DichloromethaneHCID 31297Methanesulfonyl chlorideHCID 669606955-(3-hydroxypropyl)-2-methyl-5H-furo[3,2-c]pyridine-4-one

생성물 1

HCID 669605925-(3-chloropropyl)-2-methyl-5H-furo[3,2-c]pyridin-4-one

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

Methane sulfonyl chloride(0.24 ml) was added to a dichloromethane solution(10 ml) of 5-(3-hydroxypropyl)-2-methyl-5H-furo[3,2-c]pyridine-4-one (0.28 g) and triethylamine(0.45 ml). The mixture was stirred at room temperature for two days. The reaction liquid was condensed under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate: hexane=1:4→1:1). The purified product was condensed to dryness under reduced pressure to give the title compound(0.16 g) as a white amorphous solid.

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후처리

  1. customThe reaction liquid
  2. customcondensed under reduced pressure
  3. customThe residue was purified by silica gel column chromatography (ethyl acetate: hexane=1:4→1:1)
  4. customcondensed to dryness under reduced pressure

출처 및 근거

ORD 기록
ord-159f7819e68f4f8aa220902b813c3f93
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09212187B2

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