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Potassium hydroxy sulfite → HCID 73296605, 화합물

HRID 623760
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HRID 623760 반응식
[CH2:1]([N:8]1[C:12]([C:13]([F:16])([F:15])[F:14])=[C:11]([CH3:17])[C:10]([C:18]2[CH:23]=[CH:22][C:21]([Cl:24])=[CH:20][CH:19]=2)=[C:9]1[C:25]([N:27]1[CH2:32][CH2:31]S[CH2:29][CH2:28]1)=[O:26])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O[O:34][S:35]([O-:37])=O.[K+]>CO.O>[CH2:1]([N:8]1[C:12]([C:13]([F:16])([F:14])[F:15])=[C:11]([CH3:17])[C:10]([C:18]2[CH:19]=[CH:20][C:21]([Cl:24])=[CH:22][CH:23]=2)=[C:9]1[C:25]([N:27]1[CH2:28][CH2:29][S:35](=[O:37])(=[O:34])[CH2:31][CH2:32]1)=[O:26])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 23707502Potassium hydroxy sulfiteHCID 86711840HCID 86711840, 화합물

생성물 1

HCID 73296605HCID 73296605, 화합물

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매2회

실험 절차

To a suspension of (1-benzyl-3-(4-chlorophenyl)-4-methyl-5-(trifluoromethyl)-1H-pyrrol-2-yl)(thiomorpholino)methanone (162 mg, 0.34 mmol) in MeOH (4 mL) and H2O (1 mL) was added oxone (624 mg, 1.015 mmol). The reaction mixture was stirred at room temperature overnight. The reaction mixture was diluted with H2O and extracted with DCM (60 mL). The organic layer was washed with brine, dried (Na2SO4) and purified by flash column chromategraphy (silica, heptane/EtOAc, 4:1→3:2) to give SC-26 (66 mg, 38%) as a white solid.

후처리

  1. extractionextracted with DCM (60 mL)
  2. washThe organic layer was washed with brine
  3. dry with materialdried (Na2SO4)
  4. custompurified by flash column chromategraphy (silica, heptane/EtOAc, 4:1→3:2)
  5. customto give SC-26 (66 mg, 38%) as a white solid

출처 및 근거

ORD 기록
ord-edd7dbbebc414c9faa6ed102477f8caa
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09302988B2

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