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Sulfuryl chloride → Quinaldic Acid

HRID 1861628
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HRID 1861628 반응식
C(OC(=O)N[C@H:8]([C:13](=O)[NH:14][CH:15]1[CH2:21][CH2:20][CH2:19]NC[CH:16]1[OH:22])[CH2:9][CH:10]([CH3:12])C)(C)(C)C.S(Cl)(Cl)(=O)=[O:26]>C(Cl)Cl.C([O-])(O)=O.[Na+]>[N:14]1[C:13]2[C:19](=[CH:12][CH:10]=[CH:9][CH:8]=2)[CH:20]=[CH:21][C:15]=1[C:16]([OH:22])=[O:26]
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참가 물질

5

반응물 2

HCID 24648Sulfuryl chlorideHCID 12076054HCID 12076054, 화합물

생성물 1

HCID 7124Quinaldic Acid

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 516892Sodium Bicarbonate용매2회

실험 절차

To a solution of [(S)-1-(3-hydroxy-azepan-4-ylcarbamoyl)-3-methyl-butyl]-carbamic acid tert butyl ester of Example 1g (2.5 g, 7.28 mmol) in CH2Cl2 (100 mL) and sat. NaHCO3 (400 mL) was added the solution of 2-pyridinesulfonyl chloride-N-oxide (27 mL, 102 mg/mL) dropwise in portions. As the addition proceeds additional sat. NaHCO3 is added in order to maintain the pH at approximately 8-9. Upon complete addition of the sulfonylchloride the reaction is stirred for an additional hour whereupon the organic layer was removed and washed with brine. The organic layer was evaporated and the residue chromatographed (5% methanol:dichloromethane) to provide 2.5 g of the title compound: MS (El) 500 (M+H+).

후처리

  1. additionAs the addition
  2. additionis added in order
  3. temperatureto maintain the pH at approximately 8-9
  4. customwas removed
  5. washwashed with brine
  6. customThe organic layer was evaporated
  7. customthe residue chromatographed (5% methanol:dichloromethane)

출처 및 근거

ORD 기록
ord-bfb0d094135f47f0abfa3a4227f00f23
출처 데이터셋
uspto-grants-2003_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06534498B1

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