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Sodium Hydroxide → 3-{1-[(6-Chloropyrazin-2-yl)amino]ethyl}benzoic acid

HRID 1255836
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HRID 1255836 반응식
[Cl:1][C:2]1[N:7]=[C:6]([NH:8][CH:9]([C:11]2[CH:12]=[C:13]([CH:18]=[CH:19][CH:20]=2)[C:14]([O:16]C)=[O:15])[CH3:10])[CH:5]=[N:4][CH:3]=1.[OH-].[Na+]>CO.ClCCl>[Cl:1][C:2]1[N:7]=[C:6]([NH:8][CH:9]([C:11]2[CH:12]=[C:13]([CH:18]=[CH:19][CH:20]=2)[C:14]([OH:16])=[O:15])[CH3:10])[CH:5]=[N:4][CH:3]=1
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참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 86641858Methyl 3-{1-[(6-chloropyrazin-2-yl)amino]ethyl}benzoate

생성물 1

HCID 866418593-{1-[(6-Chloropyrazin-2-yl)amino]ethyl}benzoic acid수율 41%

시약·촉매·용매 2

HCID 887Methanol용매HCID 6344Dichloromethane용매

실험 절차

A mixture of methyl 3-{1-[(6-chloropyrazin-2-yl)amino]ethyl}benzoate (30 mg, 0.1 mmol) in dilute aqueous sodium hydroxide (0.5 mL, 2M, 1 mmol), methanol (2 mL) and dichloromethane (1 mL) was stirred at room temperature for 16 hours. After this time the mixture was concentrated under reduced pressure and the residue was dissolved in water (5 mL) which was then acidified to pH 6 with dilute aqueous hydrochloric acid (1M). The aqueous solution was extracted with ethyl acetate (3×10 mL) and the extracts were washed with brine (10 mL), dried (MgSO4) and concentrated under reduced pressure to give 3-{1-[(6-chloropyrazin-2-yl)amino]ethyl}benzoic acid (11 mg, 41%) as a beige coloured oil.

후처리

  1. concentrationAfter this time the mixture was concentrated under reduced pressure
  2. dissolutionthe residue was dissolved in water (5 mL) which
  3. extractionThe aqueous solution was extracted with ethyl acetate (3×10 mL)
  4. washthe extracts were washed with brine (10 mL)
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-fb086155d60a48f8800961d82b34f110
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08461161B2

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