Hydrochloric Acid → 2-(4-fluorophenyl)-3,4-dihydro-2H-1,4-benzothiazine

HRID 1198435

반응식

HRID 1198435 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[C:13](=O)[NH:12][C:11]3[CH:15]=[CH:16][CH:17]=[CH:18][C:10]=3[S:9]2)=[CH:4][CH:3]=1.[BH4-].[Na+].Cl.C(=O)([O-])[O-].[K+].[K+]>O1CCCC1>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]2[CH2:13][NH:12][C:11]3[CH:15]=[CH:16][CH:17]=[CH:18][C:10]=3[S:9]2)=[CH:6][CH:7]=1

참가 물질

6

실험 절차

To a mixture of 2-(4-fluorophenyl)-3-oxo-3,4-dihydro-2H-1,4-benzothiazine (4.0 g), sodium borohydride (2.91 g) and tetrahydrofuran (100 ml) is added dropwise with stirring boron trifluoride etherate complex (12. 5 ml) at room temperature, and the mixture is refluxed for 1.5 hour. After cooling, to the mixture is added dropwise 10% hydrochloric acid (35 ml), and the mixture is further refluxed for one hour. The reaction mixture is poured into ice water and made alkaline with potassium carbonate and extracted with ethyl acetate. The ethyl acetate layer is washed, dried and distilled to remove the solvent. The residue is recrystallized from isopropyl ether to give 2-(4-fluorophenyl)-3,4-dihydro-2H-1,4-benzothiazine (3.45 g, yield 91%) as crystals.

후처리

  1. additionis added dropwise with stirring boron trifluoride etherate complex (12. 5 ml) at room temperature
  2. temperaturethe mixture is refluxed for 1.5 hour
  3. temperatureAfter cooling, to the mixture
  4. temperaturethe mixture is further refluxed for one hour
  5. extractionextracted with ethyl acetate
  6. washThe ethyl acetate layer is washed
  7. customdried
  8. distillationdistilled
  9. customto remove the solvent
  10. customThe residue is recrystallized from isopropyl ether

출처 및 근거

ORD 기록
ord-6f2afebbac264ddeb38dfa8207da9a4d
출처 데이터셋
uspto-grants-1994_01
특허 번호
US05281592

연결된 노트

불러오는 중…