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4-Toluenesulfonyl chloride → HCID 90388503, 화합물

HRID 2205236
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HRID 2205236 반응식
[S:1]1[C:9]2[C:8](=[O:10])[CH2:7][N:6]=[CH:5][C:4]=2[CH:3]=[CH:2]1.[H-].[Na+].[S:13](Cl)([C:16]1[CH:22]=[CH:21][C:19]([CH3:20])=[CH:18][CH:17]=1)(=[O:15])=[O:14]>C1COCC1>[CH3:20][C:19]1[CH:21]=[CH:22][C:16]([S:13]([O:10][C:8]2[C:9]3[S:1][CH:2]=[CH:3][C:4]=3[CH:5]=[N:6][CH:7]=2)(=[O:15])=[O:14])=[CH:17][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 73974-Toluenesulfonyl chlorideHCID 24758Sodium hydrideHCID 21997827HCID 21997827, 화합물

생성물 1

HCID 90388503HCID 90388503, 화합물수율 81%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of thieno[3,2-c]pyridin-7(6H)-one (110 mg, 0.728 mmol, 1.0 equiv) in THF (5.00 mL) was added NaH (35 mg, 0.873 mmol, 1.2 equiv) followed by TsCl (180 mg, 0.946 mmol, 1.3 equiv). The reaction mixture was stirred at rt for 2 h, then quenched with water and extracted with ethyl acetate. Purification by column chromatography using 20% ethyl acetate in hexanes elution gave 180 mg of a white solid, 81%.

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후처리

  1. customquenched with water
  2. extractionextracted with ethyl acetate
  3. customPurification by column chromatography
  4. wash20% ethyl acetate in hexanes elution

출처 및 근거

ORD 기록
ord-4df3ea75a75f42169c40d8cca1e386d4
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09370515B2

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