Chloroacetonitrile → HCID 14279665, 화합물

HRID 1381817노트

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HRID 1381817 반응식
[F:1][C:2]1[C:12]([N:13]2[C:21](=[O:22])[C:20]3[CH2:19][CH2:18][CH2:17][CH2:16][C:15]=3[C:14]2=[O:23])=[CH:11][C:5]2[NH:6][C:7](=[O:10])[CH2:8][O:9][C:4]=2[CH:3]=1.C(=O)([O-])[O-].[K+].[K+].Cl[CH2:31][C:32]#[N:33]>C(#N)C>[F:1][C:2]1[C:12]([N:13]2[C:21](=[O:22])[C:20]3[CH2:19][CH2:18][CH2:17][CH2:16][C:15]=3[C:14]2=[O:23])=[CH:11][C:5]2[N:6]([CH2:31][C:32]#[N:33])[C:7](=[O:10])[CH2:8][O:9][C:4]=2[CH:3]=1

참가 물질

5

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온도
5 °C

실험 절차

A suspension of 2-[7-fluoro-2H-1,4-benzoxazin-3(4H)-on-6-yl]-4,5,6,7-tetrahydro-2H-isoindole-1,3-dione (2 g) and potassium carbonate (1.05 g) in acetonitrile (30 ml) is refluxed for 30 minutes. The resulting solution is cooled to a temperature of 5° C. To the solution is added dropwise chloroacetonitrile (0.72 g), and thereafter the solution is refluxed for 3 hours. The solvent is distilled off, and the residue is admixed with water and subjected to an extraction operation with the aid of dichloromethane. The dichloromethane layer is separated off, washed with water, and dried over sodium sulfate. The solution is concentrated to precipitate a crystalline product, which is then recrystallized in a solvent consisting of acetonitrile and water. As an end product, 2-[7-fluoro-4-cyanomethyl-2H-1,4-benzoxazin-3(4H)-on-6-yl]-4,5,6,7-tetrahydro-2H-isoindole-1,3-dione (0.84 g) is obtained. mp. 216°-220° C.

후처리

  1. temperatureis refluxed for 30 minutes
  2. temperaturethe solution is refluxed for 3 hours
  3. distillationThe solvent is distilled off
  4. customThe dichloromethane layer is separated off
  5. washwashed with water
  6. dry with materialdried over sodium sulfate
  7. concentrationThe solution is concentrated
  8. customto precipitate a crystalline product, which
  9. customis then recrystallized in a solvent

출처 및 근거

ORD 기록
ord-6932387b295e4072bd3e5db202965271
출처 데이터셋
uspto-grants-1989_02
특허 번호
US04804394

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