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Sodium Bicarbonate → 6-(2-Thienyl)-2-methyl-1,4-benzoxazin-3-(4h)-one

HRID 840369
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인쇄 미리보기

반응식

HRID 840369 반응식
Br[C:2]1[CH:3]=[CH:4][C:5]2[O:10][CH:9]([CH3:11])[C:8](=[O:12])[NH:7][C:6]=2[CH:13]=1.[S:14]1[CH:18]=[CH:17][CH:16]=[C:15]1B(O)O.C(=O)(O)[O-].[Na+]>COCCOC.C(OCC)(=O)C>[S:14]1[CH:18]=[CH:17][CH:16]=[C:15]1[C:2]1[CH:3]=[CH:4][C:5]2[O:10][CH:9]([CH3:11])[C:8](=[O:12])[NH:7][C:6]=2[CH:13]=1
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참가 물질

6

반응물 3

HCID 516892Sodium BicarbonateHCID 27339602-Thiopheneboronic acidHCID 226229036-bromo-2-methyl-3,4-dihydro-2H-1,4-benzoxazin-3-one

생성물 1

HCID 226229196-(2-Thienyl)-2-methyl-1,4-benzoxazin-3-(4h)-one수율 33%

시약·촉매·용매 2

HCID 80711,2-Dimethoxyethane용매
HCID 8857
Ethyl Acetate
용매

반응 조건

온도
100 °C

실험 절차

315 mg of 6-bromo-2-methyl-1,4-benzoxazin-3-(4H)-one is mixed in 4 ml of DME with 0.2 g of 2-thiopheneboronic acid and 150 mg of tetrakis-triphenylphosphine-palladium (O) and 340 mg of sodium bicarbonate (dissolved in 4 ml of water). It is stirred for some time at 100° C. The product is diluted with ethyl acetate, extracted 3 times with water, and dried with magnesium sulfate. It is concentrated by evaporation. The crude product is purified by column chromatography with a hexane/ethyl acetate mixture and yields pure 33% product.

후처리

  1. extractionextracted 3 times with water
  2. dry with materialdried with magnesium sulfate
  3. concentrationIt is concentrated by evaporation
  4. customThe crude product is purified by column chromatography with a hexane/ethyl acetate mixture

출처 및 근거

ORD 기록
ord-32bf2a6a5f0846fb80338bb81efe33f4
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06365736B1

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