Oxalyl chloride → 2-(4-Fluorophenyl)acetyl isocyanate

HRID 2114016ノート

反応式

HRID 2114016 の反応式
FC1C=CC(CC(N)=O)=CC=1.C(Cl)(=O)C(Cl)=O.[F:18][C:19]1[CH:24]=[CH:23][C:22]([CH2:25][C:26]([NH:28][C:29](=O)[O:30]C)=[O:27])=[CH:21][CH:20]=1>ClC(Cl)C>[F:18][C:19]1[CH:20]=[CH:21][C:22]([CH2:25][C:26]([N:28]=[C:29]=[O:30])=[O:27])=[CH:23][CH:24]=1

参加物

5

反応条件

温度
80 °C

実験手順

To a solution/suspension of 4-fluorophenylacetamide (77 mg, 0.50 mmol, see generally, J. Med. Chem. 2003, 46, 4333-4341, the disclosure of which is herein incorporated by referene) in dichloroethane (2 mL) was added oxalyl chloride (0.175 mL, 2.00 mmol). The reaction was heated at 80° C. for 24 h and then 70° C. for two days. By this time, most of the solids had dissolved and the reaction was yellow. LC/MS analysis found a peak with a molecular weight of 211 corresponding to methyl 2-(4-fluorophenyl)acetylcarbamate, resulting from quenching of the isocyanate with methanol. The reaction was concentrated in vacuo to give a yellow slurry. The slurry was redissolved in dichloroethane (2 mL) and again concentrated in vacuo. The resulting residue was redissolved again in dichloroethane (2 mL) to give a 0.25 M solution of 2-(4-fluorophenyl)acetyl isocyanate in dichloroethane, which was used directly in subsequent reactions.

後処理

  1. dissolutionBy this time, most of the solids had dissolved
  2. customresulting
  3. customfrom quenching of the isocyanate with methanol
  4. concentrationThe reaction was concentrated in vacuo
  5. customto give a yellow slurry
  6. concentrationagain concentrated in vacuo
  7. dissolutionThe resulting residue was redissolved again in dichloroethane (2 mL)

出典と根拠

ORDレコード
ord-4b3ef6bbb10f436e80743ad1b9713f27
出典データセット
uspto-grants-2008_10
特許番号
US07432373B2

反応ノート

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