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Water → HCID 21099479, 화합물

HRID 1351693
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HRID 1351693 반응식
F[C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1/[CH:9]=[CH:10]/[C:11]1[CH:16]=[CH:15][C:14]([S:17]([C:20]2[CH:27]=[CH:26][CH:25]=[CH:24][C:21]=2[CH:22]=O)(=[O:19])=[O:18])=[CH:13][CH:12]=1.[CH3:28][C:29]([S:32]([NH2:34])=[O:33])([CH3:31])[CH3:30].[BH4-].[Na+].O>O1CCCC1.[O-]CC.[Ti+4].[O-]CC.[O-]CC.[O-]CC.ClCCl>[CH3:28][C:29]([S:32]([NH:34][CH2:22][C:21]1[CH:24]=[CH:25][CH:26]=[CH:27][C:20]=1[S:17]([C:14]1[CH:13]=[CH:12][C:11](/[CH:10]=[CH:9]/[C:3]2[CH:4]=[CH:5][C:6]([F:8])=[CH:7][CH:2]=2)=[CH:16][CH:15]=1)(=[O:18])=[O:19])=[O:33])([CH3:31])[CH3:30]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 962WaterHCID 3382465Tert-ButanesulfinamideHCID 4311764Sodium borohydrideHCID 21099432HCID 21099432, 화합물

생성물 1

HCID 21099479HCID 21099479, 화합물

시약·촉매·용매 3

HCID 76524Titanium tetraethoxide촉매
HCID 6344
Dichloromethane
용매
HCID 8028Tetrahydrofuran용매

실험 절차

A mixture of 2-({4-[(E)-2-(2,4-difluorophenyl)vinyl]phenyl}sulfonyl)benzaldehyde (Example 176, 500 mg, 1.44 mmol), 2-methyl-2-propanesulfinamide (192 mg, 1.58 mmol) and titanium(IV) ethoxide (0.6 mL, 2.88 mmol) in tetrahydrofuran (7 mL) was heated to reflux for 4 hours. The cooled reaction mixture was partitioned between ethyl acetate and brine. The organic layer was dried over MgSO4 and evaporated in vacuo. The residue was taken up in methanol/dichloromethane (3:1, 16 mL) and sodium borohydride (424 mg, 8.64 mmol) added portionwise. After stirring at room temperature for 10 minutes, water and dichloromethane were added. The organic layer was dried over MgSO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica, eluting with 50–90% ethyl acetate/isohexane, followed by recrystallisation to give the title compound as a white solid. δH (500 MHz, d6 DMSO): 8.11 (1H, d, J=7.8 Hz), 7.84–7.80 (4H, m), 7.73–7.66 (4H, m), 7.59–7.57 (1H, m), 7.45 (1H, d, J=16.4 Hz), 7.30 (1H, d, J=16.5 Hz), 7.23 (2H, t, J=8.8 Hz), 5.78 (1H, t, J=6.4 Hz), 4.45–4.35 (2H, m), 1.07 (9H, s).

후처리

  1. temperaturewas heated
  2. temperatureto reflux for 4 hours
  3. customThe cooled reaction mixture
  4. customwas partitioned between ethyl acetate and brine
  5. dry with materialThe organic layer was dried over MgSO4
  6. customevaporated in vacuo
  7. dry with materialThe organic layer was dried over MgSO4
  8. concentrationconcentrated in vacuo
  9. customThe residue was purified by flash column chromatography on silica
  10. washeluting with 50–90% ethyl acetate/isohexane
  11. customfollowed by recrystallisation

출처 및 근거

ORD 기록
ord-cc6c866be6e54ff9954ff9947becbf50
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07217740B2

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