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Tetrahydrofuran → HCID 13433423, 화합물

HRID 1839157
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HRID 1839157 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5](SC(C)C)=[N:6][CH:7]=1.O[O:13][S:14]([O-:16])=O.[K+].C(=O)(O)[O-].[Na+].O1C[CH2:26][CH2:25][CH2:24]1>CO>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([S:14]([CH:25]([CH3:26])[CH3:24])(=[O:16])=[O:13])=[N:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8028TetrahydrofuranHCID 516892Sodium BicarbonateHCID 134334105-Bromo-2-(isopropylthio)pyridineHCID 23707502Potassium hydroxy sulfite

생성물 1

HCID 13433423HCID 13433423, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

To a solution of 5-bromo-2-isopropylthiopyridine from Step 1 (2.03 g, 8.75 mmol) in tetrahydrofuran (50 ml) and methanol (25 ml) at 0° C. was added oxone (15.8 g, 25.8 mmol) and then saturated aqueous sodium bicarbonate (25 ml). The resulting mixture was stirred at room temperature for 6 hours. The mixture was quenched with aqueous sodium bicarbonate and partitioned between ethyl acetate and water. The crude product from the organic phase was chromatographed on silica gel eluting with 20% ethyl acetate in hexane to afford the 5-Bromo-2-isopropylsulfonylpyridine compound as a white solid.

후처리

  1. customThe mixture was quenched with aqueous sodium bicarbonate
  2. custompartitioned between ethyl acetate and water
  3. customThe crude product from the organic phase was chromatographed on silica gel eluting with 20% ethyl acetate in hexane

출처 및 근거

ORD 기록
ord-cc982e757a9944968a545b51c55fbdbc
출처 데이터셋
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06677351B2

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