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5-Chloropyrazinoic acid → 5-(Oxetan-2-ylmethoxy)pyrazine-2-carboxylic acid

HRID 571744
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HRID 571744 반응식
Cl[C:2]1[N:3]=[CH:4][C:5]([C:8]([OH:10])=[O:9])=[N:6][CH:7]=1.[O:11]1[CH2:14][CH2:13][CH:12]1[CH2:15][OH:16].CC(C)([O-])C.[K+]>CN(C)C=O>[O:11]1[CH2:14][CH2:13][CH:12]1[CH2:15][O:16][C:2]1[N:3]=[CH:4][C:5]([C:8]([OH:10])=[O:9])=[N:6][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 4654725-Chloropyrazinoic acidHCID 12284142(Oxetan-2-yl)methanolHCID 23665647Potassium tert-butoxide

생성물 1

HCID 1177383715-(Oxetan-2-ylmethoxy)pyrazine-2-carboxylic acid수율 221.7%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
120 °C

실험 절차

In a microwave vial 5-chloropyrazine-2-carboxylic acid (100.0 mg, 0.631 mmol), dimethylformamide (5 mL), oxetan-2-ylmethanol (83.4 mg, 0.946 mmol) and potassium tert-butoxide (176.9 mg, 1.58 mmol) are added. A small exotherm is observed. After 1 minute at room temperature the vial is sealed and the mixture heated at 120° C. for 30 minutes in the microwave. The reaction mixture is then quenched with aqueous NH4Cl and the solvent evaporated under reduced pressure. The resultant residue is triturated in 2-propanol. The filtrate is concentrated under reduced pressure to give the title compound as a cream solid (0.294 g, 99%) and is used without further purification. ES/MS (m/e): 211.0 (M+1), 208.8 (M−H).

후처리

  1. customAfter 1 minute at room temperature the vial is sealed
  2. customThe reaction mixture is then quenched with aqueous NH4Cl
  3. customthe solvent evaporated under reduced pressure
  4. customThe resultant residue is triturated in 2-propanol
  5. concentrationThe filtrate is concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-5e8954cb5c7647bbb4d1d8c8501e4832
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09029367B2

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