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Sodium Bicarbonate → HCID 11117620, 화합물

HRID 398831
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HRID 398831 반응식
C([NH:7][C:8]1[C:13]([C:14](O)([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH2:15][C:16](OC(C)(C)C)=[O:17])=[CH:12][CH:11]=[CH:10][N:9]=1)(=O)C(C)(C)C.C(=O)(O)[O-].[Na+]>Cl.O1CCOCC1>[C:23]1([C:14]2[C:13]3[C:8](=[N:9][CH:10]=[CH:11][CH:12]=3)[NH:7][C:16](=[O:17])[CH:15]=2)[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 516892Sodium BicarbonateHCID 10971347Tert-butyl 2-pivaloylamino-beta-hydroxy-beta-phenyl-3-pyridinepropanoate

생성물 1

HCID 11117620HCID 11117620, 화합물수율 51.4%

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 312751,4-Dioxane용매

실험 절차

Tert-butyl 2-pivaloylamino-β-hydroxy-β-phenyl-3-pyridinepropanoate (2.09 g, 5.25 mmol) was dissolved in a mixed solvent of 3N hydrochloric acid aqueous solution (10 ml) and dioxane (10 ml), and the solution was heated under reflux for 3 days. After cooling to room temperature, saturated sodium bicarbonate aqueous solution was added for neutralization. The reaction mixture was filtered, and the resulting crystals were thoroughly washed with water and recrystallized from acetonitrile to give 4-phenyl-1,8-naphthyridin-2(1H)-one (600 mg, 51%).

후처리

  1. temperaturethe solution was heated
  2. temperatureunder reflux for 3 days
  3. filtrationThe reaction mixture was filtered
  4. washthe resulting crystals were thoroughly washed with water
  5. customrecrystallized from acetonitrile

출처 및 근거

ORD 기록
ord-5401f47701eb412abe6a91350884ed53
출처 데이터셋
uspto-grants-1998_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05817670

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