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Sodium Sulfite → HCID 68685769, 화합물

HRID 2238632
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HRID 2238632 반응식
CS[C:3]1[N:8]=[C:7]([C:9]2[N:13]3[CH:14]=[CH:15][CH:16]=[CH:17][C:12]3=[N:11][CH:10]=2)[CH:6]=[CH:5][N:4]=1.Cl[C:19]1C=CC=C(C(OO)=O)C=1.[S:29]([O-:32])([O-])=[O:30].[Na+].[Na+]>C(Cl)(Cl)Cl>[CH3:19][S:29]([C:3]1[N:8]=[C:7]([C:9]2[N:13]3[CH:14]=[CH:15][CH:16]=[CH:17][C:12]3=[N:11][CH:10]=2)[CH:6]=[CH:5][N:4]=1)(=[O:32])=[O:30]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24437Sodium SulfiteHCID 70297m-Chloroperbenzoic acidHCID 20751408HCID 20751408, 화합물

생성물 1

HCID 68685769HCID 68685769, 화합물

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

150 mg of 3-[2-methylthio-4-pyrimidinyl]imidazo[1,2-a]pyridine [1-3] was dissolved in 3 mL of chloroform and 169 mg of m-chloroperbenzoic acid was added under an ice-cold condition, and stirred for 30 minutes at the same temperature. The resultant solution was added with a saturated aqueous solution of sodium sulfite and a saturated aqueous solution of sodium hydrogen carbonate, and then was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and then the insolubles were filtered, and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography, and 160 mg of 3-[2-methylsulfonyl-4-pyrimidinyl]imidazo[1,2-a]pyridine [1-4] was obtained as a colorless amorphous substance.

후처리

  1. extractiona saturated aqueous solution of sodium hydrogen carbonate, and then was extracted with chloroform
  2. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  3. filtrationthe insolubles were filtered
  4. concentrationthe filtrate was concentrated
  5. customThe obtained residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-8e330c2fae8f44e3ab4e58a46e6fdb19
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07718801B2

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