1,2-Dichloroethane → (1,3-Dihydroisobenzofuran-1-yl)-(piperidin-4-yl)methanone hydrochloride

HRID 914919노트

반응식

HRID 914919 반응식
C([N:8]1[CH2:13][CH2:12][CH:11]([C:14]([CH:16]2[C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[CH2:18][O:17]2)=[O:15])[CH2:10][CH2:9]1)C1C=CC=CC=1.[Cl:25]CCCl>ClC(OC(Cl)C)=O>[ClH:25].[CH:16]1([C:14]([CH:11]2[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]2)=[O:15])[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH2:18][O:17]1

참가 물질

4

실험 절차

After dissolving 517 mg of (1-benzylpiperidin-4-yl)-(1,3-dihydroisobenzofuran-1-yl)methanone in 5 ml of 1,2-dichloroethane, 0.49 ml of 1-chloroethyl chloroformate was added and the mixture was heated to reflux for 1 hour. The reaction solution was distilled off under reduced pressure, 5 ml of methanol was added to the residue and heating to reflux was continued for 1 hour. The reaction solution was distilled off under reduced pressure, saturated aqueous sodium bicarbonate solution was added and extraction was performed with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and then the solvent was distilled off under reduced pressure to obtain 104 mg of (1,3-dihydroisobenzofuran-1-yl)-(piperidin-4-yl)methanone hydrochloride.

후처리

  1. additionwas added
  2. temperaturethe mixture was heated
  3. temperatureto reflux for 1 hour
  4. distillationThe reaction solution was distilled off under reduced pressure, 5 ml of methanol
  5. additionwas added to the residue
  6. temperatureheating
  7. temperatureto reflux
  8. distillationThe reaction solution was distilled off under reduced pressure, saturated aqueous sodium bicarbonate solution
  9. additionwas added
  10. extractionextraction
  11. dry with materialThe extract was dried over anhydrous magnesium sulfate
  12. distillationthe solvent was distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-3dcc01c440c9405586c0283bcfa08853
출처 데이터셋
uspto-grants-2007_09
특허 번호
US07265108B2

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