Hydrochloric Acid → 3-Oxo-1,3-dihydrobenzo[c]isothiazole-5-carboxylic acid

HRID 38662

반응식

HRID 38662 반응식
[S:1]([Li])[Li].Cl.O=C1[NH:11][C:10]2[CH:12]=[CH:13][C:14]([C:16]([OH:18])=[O:17])=[CH:15][C:9]=2[C:8](=O)[O:7]1>O>[O:7]=[C:8]1[S:1][NH:11][C:10]2[CH:12]=[CH:13][C:14]([C:16]([OH:18])=[O:17])=[CH:15][C:9]1=2

참가 물질

5

실험 절차

To a solution of Li2S (5.7 g, 0.124 mol) in H2O (1000 ml) cooled to 0° C. in an ice bath was added HCl (1M, 186 ml, 0.186 mmol) slowly with stirring. The ice bath was then removed, and 2,4-dioxo-2,4-dihydro-1H-benzo[d][1,3]oxazine-6-carboxylic acid (8.1 g, 0.050 mol) was added slowly. The suspension was stirred for 1 h and was filtered. The filtrate was purged with N2 for 30 min, and H2O2 (30%, 7.0 ml) was added, stirred for 45 min. The pH of the reaction mixture was adjusted with 6M HCl to ˜5 and the resulting suspension was filtered. The solid was washed with H2O (×3) and was dried to yield 3-oxo-1,3-dihydrobenzo[c]isothiazole-5-carboxylic acid as an off-white solid. To a solution of 3-oxo-1,3-dihydrobenzo[c]isothiazole-5-carboxylic acid 4.2 g, 27.8 mmol) in acetone (100 ml) was added MeI (5.2 ml, 83.4 mmol) and K2CO3 (7.7 g, 55.6 mmol). The mixture was heated to 60° C. for 2 h, and was filtered and concentrated. The crude product was purified by flash column chromatography on silica gel eluting with 20%→30% EtOAc-hexane to yield Intermediate 9 as a yellow solid.

후처리

  1. customThe ice bath was then removed
  2. stirringThe suspension was stirred for 1 h
  3. filtrationwas filtered
  4. customThe filtrate was purged with N2 for 30 min
  5. additionH2O2 (30%, 7.0 ml) was added
  6. stirringstirred for 45 min
  7. filtrationthe resulting suspension was filtered
  8. washThe solid was washed with H2O (×3)
  9. customwas dried

출처 및 근거

ORD 기록
ord-1df6df290fde4cd894957272816ef663
출처 데이터셋
uspto-grants-2013_09
특허 번호
US08524745B2

연결된 노트

불러오는 중…