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Water → N-(5-(5-formylfuran-2-yl)-4-methylthiazol-2-yl)acetamide

HRID 2386175
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HRID 2386175 반응식
Br[C:2]1[S:6][C:5]([NH:7][C:8](=[O:10])[CH3:9])=[N:4][C:3]=1[CH3:11].[CH:12]([C:14]1[O:18][C:17](B(O)O)=[CH:16][CH:15]=1)=[O:13].C(=O)(O)[O-].[Na+].O>CN1C(=O)CCC1.[Pd](Cl)Cl>[CH:12]([C:14]1[O:18][C:17]([C:2]2[S:6][C:5]([NH:7][C:8](=[O:10])[CH3:9])=[N:4][C:3]=2[CH3:11])=[CH:16][CH:15]=1)=[O:13]
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참가 물질

7

반응물 4

HCID 962WaterHCID 516892Sodium BicarbonateHCID 822437N-(5-bromo-4-methyl-1,3-thiazol-2-yl)acetamideHCID 27343555-Formylfuran-2-boronic acid

생성물 1

HCID 14532745N-(5-(5-formylfuran-2-yl)-4-methylthiazol-2-yl)acetamide수율 37.6%

시약·촉매·용매 2

HCID 24290
Palladium Chloride
촉매
HCID 13387N-methyl-2-pyrrolidone용매

실험 절차

To a solution of 3.0 g of N-(5-bromo-4-methylthiazol-2-yl)acetamide in 50 mL of NMP was added 3.0 g of 5-formylfuran-2-ylboronic acid. To the stirred solution was then added 300 mg of 1,1 bis-(diphenylphosphino)-ferrocene) palladium dichloride followed by 10 mL of saturated sodium bicarbonate. The resulting biphasic mixture was irradiated at 150° C. in a microwave for 20 min. The resulting mixture was poured into 200 mL of water and filtered. The filtrate was extracted with ether and the ether layers were combined, dried over sodium sulfate and concentrated. The resulting oil was precipitated with methylene chloride and filtered, yielding 1.2 g of N-(5-(5-formylfuran-2-yl)-4-methylthiazol-2-yl)acetamide as an orange solid which was used without further purification. LC/MS: 251.07 (M+H)/2.18 min.

후처리

  1. customThe resulting biphasic mixture was irradiated at 150° C. in a microwave for 20 min
  2. filtrationfiltered
  3. extractionThe filtrate was extracted with ether
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated
  6. customThe resulting oil was precipitated with methylene chloride
  7. filtrationfiltered

출처 및 근거

ORD 기록
ord-bd27cf2b1efd4a50a4358e2fa564ac30
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08268818B2

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