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2-Chloroethyl chloroformate → 2-(5-Phenyl-1,2,4-oxadiazol-3-yl)morpholine hydrochloride

HRID 2063356
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HRID 2063356 반응식
C([N:8]1[CH2:13][CH2:12][O:11][CH:10]([C:14]2[N:18]=[C:17]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[O:16][N:15]=2)[CH2:9]1)C1C=CC=CC=1.[Cl:25]C(OCCCl)=O>ClCCCl>[ClH:25].[C:19]1([C:17]2[O:16][N:15]=[C:14]([CH:10]3[O:11][CH2:12][CH2:13][NH:8][CH2:9]3)[N:18]=2)[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1
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참가 물질

4

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HCID 123052-Chloroethyl chloroformateHCID 580978824-Benzyl-2-(5-phenyl-1,2,4-oxadiazol-3-yl)morpholine2회

생성물 1

HCID 668424982-(5-Phenyl-1,2,4-oxadiazol-3-yl)morpholine hydrochloride

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

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온도
70 °C

실험 절차

To a stirred solution of 4-benzyl-2-(5-phenyl-1,2,4-oxadiazol-3-yl)morpholine (intermediate 27, 900 mg, 2.80 mmol) in 1,2-dichloroethane (2.0 ml) was added chloroethyl chloroformate (0.46 ml, 4.20 mmol), and the reaction mixture was stirred at 70° C. for 4 hours. The reaction mixture was concentrated in vacuo. After removal of the solvent, the residue was dissolved in methanol (2.0 ml), and the solution was stirred under reflux for one hour. When the reaction was complete (checked by thin layer chromatography), the reaction mixture was concentrated in vacuo. The resulting 2-(5-phenyl-[1,2,4]oxadiazol-3-yl)-morpholine hydrochloride (intermediate 28) was used for next reaction without further purification.

후처리

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. customAfter removal of the solvent
  3. dissolutionthe residue was dissolved in methanol (2.0 ml)
  4. stirringthe solution was stirred
  5. temperatureunder reflux for one hour
  6. concentrationthe reaction mixture was concentrated in vacuo
  7. customThe resulting 2-(5-phenyl-[1,2,4]oxadiazol-3-yl)-morpholine hydrochloride (intermediate 28) was used for next reaction without further purification

출처 및 근거

ORD 기록
ord-474c773cf3eb4410920469d20b88634b
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08288383B2

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