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Ethyl propiolate → Ethyl 4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine-2-carboxylate

HRID 2307252
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인쇄 미리보기

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HRID 2307252 반응식
[N:1]1O[C:3]([O-])=[C:4]2[CH2:9][CH2:8][CH2:7][CH2:6][N+:5]=12.[C:11]([O:15][CH2:16][CH3:17])(=[O:14])[C:12]#C>C1(C)C(C)=CC=CC=1>[N:1]1[N:5]2[CH2:6][CH2:7][CH2:8][CH2:9][C:4]2=[CH:3][C:12]=1[C:11]([O:15][CH2:16][CH3:17])=[O:14]
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참가 물질

4

반응물 2

HCID 12182Ethyl propiolateHCID 118450904,5,6,7-Tetrahydro-(1,2,3)oxadiazolo(3,4-a)pyridin-8-ium-3-olate

생성물 1

HCID 11845784Ethyl 4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine-2-carboxylate

시약·촉매·용매 1

HCID 7237O-Xylene용매

실험 절차

A mixture of 4,5,6,7-tetrahydro[1,2,3]oxadiazolo[3,4-a]pyridin-8-ium-3-olate (Heterocycles; 1990; 31; 481), (13.0 g, 93 mmol), and ethyl propiolate (28.5 ml, 278 mmol), in xylene (250 ml) was heated under reflux for 2 hours. The cooled mixture was evaporated under reduced pressure. The residual oil was purified by column chromatography on silica gel using ether as the eluant, to afford the title compound as an oil, 5.82 g.

후처리

  1. temperatureunder reflux for 2 hours
  2. customThe cooled mixture was evaporated under reduced pressure
  3. customThe residual oil was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-19fbf650ee5f4366b4dd40ced2f44c0a
출처 데이터셋
uspto-grants-2004_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06831074B2

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