Sulfuric Acid → 3-(4-Chlorobenzyl)-3-formamidocyclobutanecarboxylic acid

HRID 1778596노트

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HRID 1778596 반응식
[Cl:1][C:2]1[CH:16]=[CH:15][C:5]([CH2:6][C:7]2(O)[CH2:10][CH:9]([C:11]([OH:13])=[O:12])[CH2:8]2)=[CH:4][CH:3]=1.[C-]#[N:18].[K+].OS(O)(=O)=O.[C:25]([OH:31])(C(F)(F)F)=O>>[Cl:1][C:2]1[CH:16]=[CH:15][C:5]([CH2:6][C:7]2([NH:18][CH:25]=[O:31])[CH2:10][CH:9]([C:11]([OH:13])=[O:12])[CH2:8]2)=[CH:4][CH:3]=1

참가 물질

5

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온도
0 °C

실험 절차

A solution of 3-(4-chlorobenzyl)-3-hydroxycyclobutanecarboxylic acid (1 g, 4.17 mmol) in TFA (17.5 mL) was charged with KCN (813 mg, 12.5 mmol), cooled to 0° C. and treated with H2SO4 (3.5 mL) dropwise. The cooling bath was removed and stirring was continued for 1.5 h. Once the reaction was complete, the mixture was re-cooled to 0° C. diluted with water, and extracted with diethyl ether. The organic layer was washed successively with 1M NaOH and saturated aqueous sodium chloride. The solution was dried over MgSO4, filtered and concentrated. Purification by flash column chromatography (gradient 1-20% methanol in dichloromethane) afforded the subject compound (500 mg, 45% yield). 1H NMR (DMSO-d6, 600 MHz) δ 12.15 (bs, 1H), 8.38 (s, 1H), 7.88 (d, J=1.13 Hz, 1H), 7.36-7.32 (m, 4H), 2.94-2.89 (m, 1H), 2.57-2.53 (m, 1H), 2.36-2.32 (m, 1H), 2.26-2.22 (m, 1H), 2.03-1.96 (m, 1H), 1.95-1.88 (m, 2H). ESI MS found for C13H14ClNO3 m/z [266.1 (M−1)].

후처리

  1. customThe cooling bath was removed
  2. temperaturethe mixture was re-cooled to 0° C.
  3. additiondiluted with water
  4. extractionextracted with diethyl ether
  5. washThe organic layer was washed successively with 1M NaOH and saturated aqueous sodium chloride
  6. dry with materialThe solution was dried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customPurification by flash column chromatography (gradient 1-20% methanol in dichloromethane)

출처 및 근거

ORD 기록
ord-18be15a21d7f4e07adde8fbaa26048fc
출처 데이터셋
uspto-grants-2016_02
특허 번호
US09266908B2

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