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Acetyl chloride → HCID 178474038、化合物

HRID 1615717
ノート
印刷プレビュー

反応式

HRID 1615717 の反応式
[F:1][C:2]1[CH:3]=[C:4]([C:8]2[CH:12]=[C:11]([NH2:13])[NH:10][N:9]=2)[CH:5]=[CH:6][CH:7]=1.CN1CC[O:18][CH2:17][CH2:16]1.C(Cl)(=O)C>C(Cl)Cl>[F:1][C:2]1[CH:3]=[C:4]([C:8]2[CH:12]=[C:11]([NH:13][C:17](=[O:18])[CH3:16])[NH:10][N:9]=2)[CH:5]=[CH:6][CH:7]=1
参加物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 6367Acetyl chlorideHCID 79724-MethylmorpholineHCID 178507283HCID 178507283、化合物

生成物 1

HCID 178474038HCID 178474038、化合物収率 96.3%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of 3-(3-fluorophenyl)-1H-pyrazol-5-amine (6.5 g, 36 mmol) and N-methylmorpholine (9.7 mL, 88 mmol) in CH2Cl2 (150 mL) was added acetyl chloride (6 mL, 85 mmol) dropwise at 0° C. under an atmosphere of nitrogen. The reaction mixture was stirred at room temperature for 1 d. The reaction mixture was concentrated in vacuo. MeOH (50 mL) and THF (50 mL) were added to the residue, followed by the addition of NaOH solution (aq. 2.5 M, 42.5 mL) at 0° C. The reaction mixture was stirred at room temperature for 15 min and HCl solution was added until pH reached ˜6. The organic solvents were evaporated in vacuo. The solid from the resulting aqueous suspension was collected by filtration, yielding the title compound as a solid (7.6 g).

後処理

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. additionMeOH (50 mL) and THF (50 mL) were added to the residue
  3. additionfollowed by the addition of NaOH solution (aq. 2.5 M, 42.5 mL) at 0° C
  4. stirringThe reaction mixture was stirred at room temperature for 15 min
  5. additionHCl solution was added until pH
  6. customThe organic solvents were evaporated in vacuo
  7. filtrationThe solid from the resulting aqueous suspension was collected by filtration

出典と根拠

ORDレコード
ord-58f74570a4e94a0f9cc14af5b9af2610
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08765762B2

反応ノート

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