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Potassium Carbonate → Isoguvacine

HRID 1246694
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HRID 1246694 반응식
[NH:1]1[CH2:6][CH:5]=[C:4]([C:7]([O:9]CC)=[O:8])[CH2:3][CH2:2]1.C([O-])([O-])=O.[K+].[K+].[OH-].[Na+]>ClCCl.CO.C[O-].[Na+]>[NH:1]1[CH2:2][CH:3]=[C:4]([C:7]([OH:9])=[O:8])[CH2:5][CH2:6]1
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참가 물질

7

반응물 3

HCID 11430Potassium CarbonateHCID 14798Sodium HydroxideHCID 13859979Ethyl 1,2,3,6-tetrahydropyridine-4-carboxylate

생성물 1

HCID 3765Isoguvacine

시약·촉매·용매 3

HCID 887Methanol용매2회HCID 6344Dichloromethane용매
HCID 10942334
Sodium Methoxide
용매

실험 절차

Ethyl 1,2,3,6-tetrahydro-4-pyridinecarboxylate (44.7 g, 234 mmol) in dichloromethane (200 mL) was treated with aqueous K2CO3 (saturated) and the phases were separated. The aqueous layer was dried under reduced pressure and the residue was triturated with dichloromethane (100×3 mL) and dissolved in methanol (100 mL). The solution was treated with a saturated solution of NaOH (10 g, 250 mmol) in methanol (250 mL) and sodium methoxide in methanol (0.5M, 200 mL, 100 mmol). After stirring at room temperature for two days, the mixture was concentrated under reduced pressure. The residue was triturated with methanol (200×5 mL) and dried under reduced pressure to provide the title compound. 1H NMR (300 MHz, CD3OD) δ 6.60 (m, 1H), 3.38 (m, 2H), 2.88 (m, 2H), 2.30 (m, 2H).

후처리

  1. customthe phases were separated
  2. customThe aqueous layer was dried under reduced pressure
  3. customthe residue was triturated with dichloromethane (100×3 mL)
  4. dissolutiondissolved in methanol (100 mL)
  5. concentrationthe mixture was concentrated under reduced pressure
  6. customThe residue was triturated with methanol (200×5 mL)
  7. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-2305a52d14f44b408e76d21fa2557c2f
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07129235B2

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