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Triethylamine → Methyl 2-(ethylcarbamoyl)isonicotinate

HRID 623567
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HRID 623567 반응식
[CH3:1][O:2][C:3]([C:5]1[CH:10]=[CH:9][N:8]=[C:7]([C:11]([OH:13])=O)[CH:6]=1)=[O:4].[Cl-].[Mg+2].[Cl-].Cl.[CH2:18]([NH2:20])[CH3:19].C(N(CC)CC)C>ClCCl>[CH2:18]([NH:20][C:11]([C:7]1[CH:6]=[C:5]([CH:10]=[CH:9][N:8]=1)[C:3]([O:2][CH3:1])=[O:4])=[O:13])[CH3:19]
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참가 물질

6

반응물 4

HCID 8471TriethylamineHCID 11198Ethylamine hydrochlorideHCID 5360315Magnesium ChlorideHCID 133537524-(Methoxycarbonyl)pyridine-2-carboxylic acid

생성물 1

HCID 67509052Methyl 2-(ethylcarbamoyl)isonicotinate수율 49.2%

시약·촉매·용매 1

HCID 6344Dichloromethane
용매

실험 절차

A mixture of 4-(methoxycarbonyl)picolinic acid (1.00 g, 5.12 mmol) and magnesium chloride (312 mg, 3.28 mmol) in dichloromethane (10 mL) is stirred at room temperature for 0.5 hour. Then, ethylamine hydrochloride (627 mg, 7.69 mmol) and triethylamine (1.07 mL, 7.69 mmol) are added. After stirring at room temperature for 20 hours, the mixture is poured onto water (50 mL). The aqueous phase is extracted with EtOAc (50 mL×2). The combined organic layer is dried over sodium sulfate and concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting with n-hexane/ethyl acetate (3:11:1) to give 525 mg (49% yield) of the title compound as a white solid.

후처리

  1. stirringAfter stirring at room temperature for 20 hours
  2. additionthe mixture is poured onto water (50 mL)
  3. extractionThe aqueous phase is extracted with EtOAc (50 mL×2)
  4. dry with materialThe combined organic layer is dried over sodium sulfate
  5. concentrationconcentrated in vacuo
  6. customThe residue is purified by column chromatography on silica gel eluting with n-hexane/ethyl acetate (3:11:1)

출처 및 근거

ORD 기록
ord-0e999654a7c9400aa1777e5054e0caee
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09302991B2

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