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Hydrochloric Acid → Ethyl 5,6,7,8-tetrahydroimidazo[1,2-a]pyridine-6-carboxylate hydrochloride

HRID 1055156
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HRID 1055156 반응식
[ClH:1].[N:2]1[CH:3]=[CH:4][N:5]2[CH:10]=[C:9]([C:11]([O:13][CH3:14])=[O:12])[CH:8]=[CH:7][C:6]=12.[CH2:15](O)C>[Pd]>[ClH:1].[N:2]1[CH:3]=[CH:4][N:5]2[CH2:10][CH:9]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH2:8][CH2:7][C:6]=12
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 702EthanolHCID 2764326Methyl imidazo(1,2-a)pyridine-6-carboxylate

생성물 1

HCID 90424115Ethyl 5,6,7,8-tetrahydroimidazo[1,2-a]pyridine-6-carboxylate hydrochloride수율 88%

시약·촉매·용매 1

HCID 23938Palladium촉매

반응 조건

온도
60 °C

실험 절차

Add 5 N hydrochloric acid (100 mL; 500.00 mmoles) and ethanol (200 mL) to a flask containing methyl imidazo[1,2-a]pyridine-6-carboxylate (4.98 g; 1.0 equiv; 28.27 mmoles) and 10% palladium on carbon (3.01 g; 0.1 equiv; 2.83 mmoles). Evacuate and backfill the reaction vessel with nitrogen (3×), then re-evacuate and backfill the reaction with hydrogen (3×). Heat the reaction mixture to 60° C. and vigorously stir under a hydrogen atmosphere for 24 hours, then evacuate and backfill the reaction vessel with nitrogen (3×) and filter the reaction mixture through Celite™, rinsing the filter cake with ethanol (100 mL). Concentrate the filtrate, add toluene (200 mL), and concentrate to dryness (repeat 2 times) to afford ethyl 5,6,7,8-tetrahydroimidazo[1,2-a]pyridine-6-carboxylate hydrochloride (5.74 g; 88%) as a white solid. MS (m/z): 195(M+1).

후처리

  1. customEvacuate
  2. customre-evacuate
  3. customthe reaction with hydrogen (3×)
  4. customevacuate
  5. filtrationfilter the reaction mixture through Celite™
  6. washrinsing the filter cake with ethanol (100 mL)
  7. concentrationConcentrate the filtrate
  8. additionadd toluene (200 mL)
  9. concentrationconcentrate to dryness (repeat 2 times)

출처 및 근거

ORD 기록
ord-8b2081836c9a4cf08e2a6fc0b5f7f259
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09394317B2

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