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Sodium Hydroxide → rac-(4aR,7aR)-octahydro-1H-cyclopenta[c]pyridine-3,6-dione

HRID 2364693
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HRID 2364693 반응식
[C@@H:1]12[CH2:8][C:7](=[O:9])[CH2:6][C@@H:5]1[CH2:4][C:3](=[O:10])[CH2:2]2.[N-:11]=[N+]=[N-].[Na+].[OH-].[Na+]>Cl>[CH2:4]1[C@H:5]2[CH2:6][C:7](=[O:9])[CH2:8][C@H:1]2[CH2:2][C:3](=[O:10])[NH:11]1
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참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 33557Sodium AzideHCID 178516323HCID 178516323, 화합물

생성물 1

HCID 11030030rac-(4aR,7aR)-octahydro-1H-cyclopenta[c]pyridine-3,6-dione수율 150.7%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

(cis)-Bicyclo[3.3.0]octane-3,7-dione 14c (1.80 g, 13 mmol) was dissolved in 25 mL of concentrated hydrochloric acid in an ice-water bath, added with sodium azide (1.10 g, 16.90 mmol) in batches, then heated to room temperature and stirred for 12 hours. The reaction solution was added dropwise with 20% sodium hydroxide solution to adjust pH to 10 to 11, extracted with dichloromethane (50 mL×3). The combined organic phase was washed with saturated sodium chloride solution (50 mL×3), then dried over anhydrous magnesium sulfate, filtered and the filtrate was concentrated under reduced pressure to obtain the title compound (cis)-2,4,4a,5,7,7a-hexahydro-1H-cyclopenta[c]pyridine-3,6-dione 14d (3 g, yield: 100.0%) as a white solid.

후처리

  1. extractionextracted with dichloromethane (50 mL×3)
  2. washThe combined organic phase was washed with saturated sodium chloride solution (50 mL×3)
  3. dry with materialdried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationthe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-dc5cdccc87b94ccc9e0535a8638b70f5
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08691822B2

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