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Tert-Butyl nitrite → Ethyl 5-iodothiazole-4-carboxylate

HRID 2246071
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HRID 2246071 반응식
N[C:2]1[S:3][C:4]([I:12])=[C:5]([C:7]([O:9][CH2:10][CH3:11])=[O:8])[N:6]=1.C(ON=O)(C)(C)C>CN(C=O)C.[Cl-].[Na+].O>[CH2:10]([O:9][C:7]([C:5]1[N:6]=[CH:2][S:3][C:4]=1[I:12])=[O:8])[CH3:11]
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참가 물질

5

반응물 2

HCID 10906Tert-Butyl nitriteHCID 45117588Ethyl 2-amino-5-iodo-1,3-thiazole-4-carboxylate

생성물 1

HCID 59705069Ethyl 5-iodothiazole-4-carboxylate수율 50.1%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 57417360Sodium chloride; water용매

실험 절차

A solution of 10.68 g of 2-amino-4-ethoxycarbonyl-5-iodothiazole in 140 ml of DMF was cooled in ice under an argon atmosphere. t-Butylnitrite (6.15 ml) was added to the cooled solution, and the mixture was stirred at room temperature for 30 min. The reaction solution was poured into brine, and the mixture was extracted three times with ethyl acetate. The organic layers were combined, followed by washing three times with brine. The organic layer was dried over anhydrous magnesium sulfate, was filtered, and was concentrated under the reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=5:1 to 3:1) to give 5.08 g of 4-ethoxycarbonyl-5-iodothiazole.

후처리

  1. extractionthe mixture was extracted three times with ethyl acetate
  2. washby washing three times with brine
  3. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  4. filtrationwas filtered
  5. concentrationwas concentrated under the reduced pressure
  6. customThe residue was purified by column chromatography on silica gel (hexane:ethyl acetate=5:1 to 3:1)

출처 및 근거

ORD 기록
ord-66f8547db03d453d95e5c28d37c8bdf1
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07687490B2

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