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Hydrochloric Acid → 3-(7-Ethyl-4-oxo-4,5-dihydroimidazo[1,5-a]quinoxalin-1-yl)-propanoic acid

HRID 2068957
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반응식

HRID 2068957 반응식
[CH2:1]([C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]1[C:13]([CH2:16][CH2:17][C:18]([O:20]CC)=[O:19])=[N:14][CH:15]=[C:8]1[C:7](=[O:23])[NH:6]2)[CH3:2].Cl>C(O)C>[CH2:1]([C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]1[C:13]([CH2:16][CH2:17][C:18]([OH:20])=[O:19])=[N:14][CH:15]=[C:8]1[C:7](=[O:23])[NH:6]2)[CH3:2]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 59198574Ethyl 3-(7-ethyl-4-oxo-4,5-dihydroimidazo[1,5-a]quinoxalin-1-yl)propanoate

생성물 1

HCID 591986403-(7-Ethyl-4-oxo-4,5-dihydroimidazo[1,5-a]quinoxalin-1-yl)-propanoic acid

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a mixture of ethyl 3-(7-ethyl-4-oxo-4,5-dihydroimidazo-[1,5-a]-quinoxalin-1-yl)propanoate as synthesized in above Example 184, 50 mg and ethanol 3 mL, 1N sodium hydroxide solution 1.2 mL was added and heated under reflux for 2 hours. The reaction liquid was allowed to cool off, and to which 1N hydrochloric acid 1.2 mL was added. The precipitated crystals were recovered by filtration, washed with water and dried in flowing air to provide 37 mg of the title compound.

후처리

  1. additionwas added
  2. temperatureheated
  3. temperatureunder reflux for 2 hours
  4. customThe reaction liquid
  5. temperatureto cool off
  6. filtrationThe precipitated crystals were recovered by filtration
  7. washwashed with water
  8. customdried

출처 및 근거

ORD 기록
ord-0908aaf86ea54e4ab638ea7c46ac4933
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08299080B2

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