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Pyridine → 1-tert-Butyl 3-ethyl 3-cyanoazetidine-1,3-dicarboxylate

HRID 1175152
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HRID 1175152 반응식
[CH2:1]([O:3][C:4]([C:6]1([C:17](=O)[NH2:18])[CH2:9][N:8]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[CH2:7]1)=[O:5])[CH3:2].N1C=CC=CC=1.FC(F)(F)C(OC(=O)C(F)(F)F)=O>C1COCC1>[CH2:1]([O:3][C:4]([C:6]1([C:17]#[N:18])[CH2:9][N:8]([C:10]([O:12][C:13]([CH3:15])([CH3:14])[CH3:16])=[O:11])[CH2:7]1)=[O:5])[CH3:2]
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참가 물질

5

반응물 3

HCID 1049PyridineHCID 9845Trifluoroacetic anhydrideHCID 595583791-Tert-butyl 3-ethyl 3-carbamoylazetidine-1,3-dicarboxylate

생성물 1

HCID 595585001-tert-Butyl 3-ethyl 3-cyanoazetidine-1,3-dicarboxylate수율 94.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

3-Carbamoyl-azetidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester (25.4 g; 93.5 mmol) is dissolved in THF (260 ml) and pyridine (19.2 g; 243 mmol) and cooled to 0° C. under stirring. Trifluoroacetic acid anhydride (26.4 ml; 187 mmol) is added dropwise over 10 minutes, the mixture warmed to room temperature and stirred for 30 minutes, poured on water and extracted with TBME three times. The combined organic phases are dried over Na2SO4, filtered, evaporated and purified via chromatography (SiO2; heptane/TBME 6:4) to yield the title compound as light brown oil (22.4 g; 94%).

후처리

  1. stirringstirred for 30 minutes
  2. additionpoured on water
  3. extractionextracted with TBME three times
  4. dry with materialThe combined organic phases are dried over Na2SO4
  5. filtrationfiltered
  6. customevaporated
  7. custompurified via chromatography (SiO2; heptane/TBME 6:4)

출처 및 근거

ORD 기록
ord-ea76da750e454940960ed21e618ce667
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07838674B2

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