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

HRID 571744
ノート
印刷プレビュー

反応式

HRID 571744 の反応式
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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
120 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-5e8954cb5c7647bbb4d1d8c8501e4832
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09029367B2

反応ノート

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