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Water → Methyl 2-chloro-5-oxo-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate

HRID 2277599
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HRID 2277599 반응식
[CH3:1][O:2][C:3]([N:5]1[CH2:14][CH2:13][C:12]2[N:11]=[C:10]([Cl:15])[CH:9]=[CH:8][C:7]=2[CH2:6]1)=[O:4].CC#N.[OH2:19]>C(Cl)(Cl)(Cl)Cl>[CH3:1][O:2][C:3]([N:5]1[CH2:14][CH2:13][C:12]2[N:11]=[C:10]([Cl:15])[CH:9]=[CH:8][C:7]=2[C:6]1=[O:19])=[O:4]
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참가 물질

5

반응물 3

HCID 962WaterHCID 6342AcetonitrileHCID 58155432Methyl 2-chloro-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate

생성물 1

HCID 58155423Methyl 2-chloro-5-oxo-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate수율 60%

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

2-Chloro-7,8-dihydro-5H-[1,6]naphthyridine-6-carboxylic acid methyl ester (226.7 mg, 1 mmol) was dissolved in CCl4 (3.57 mL) and MeCN (0.357 mL) at room temperature before adding NaIO4 (0.643 g) in 1 mL of H2O, followed by RuCl3.hydrate (62.2 mg). The reaction mixture was stirred vigorously at room temperature for 2 hours. After dilution with DCM, it was filtered through Celite and the filter cake was washed three times with DCM. The combined organic solution was concentrated in vacuo to give a crude product. Flash column chromatography separation (silica gel, 12 g, 20% EtOAc in hexane) then afforded the tile compound (143 mg, 60%) as a white solid. MS: 241.1 (M+H+).

후처리

  1. filtrationAfter dilution with DCM, it was filtered through Celite
  2. washthe filter cake was washed three times with DCM
  3. concentrationThe combined organic solution was concentrated in vacuo
  4. customto give a crude product
  5. customFlash column chromatography separation (silica gel, 12 g, 20% EtOAc in hexane)

출처 및 근거

ORD 기록
ord-909dd1da8f6c4312a2fe2f5d09654d81
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09133158B2

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