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

HRID 1158861
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반응식

HRID 1158861 반응식
[C:1]([O:5][CH2:6][CH3:7])(=[O:4])[C:2]#[CH:3].[NH:8]1[N:12]2[CH2:13][CH2:14][CH2:15][CH2:16][CH:11]2C(=O)O1>CC1C=CC=CC=1C>[CH2:6]([O:5][C:1]([C:2]1[CH:3]=[C:11]2[CH2:16][CH2:15][CH2:14][CH2:13][N:12]2[N:8]=1)=[O:4])[CH3:7]
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참가 물질

4

반응물 2

HCID 12182Ethyl propiolateHCID 69656246Tetrahydropyridino[1,2-c][1,2,3]oxadiazolone

생성물 1

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

시약·촉매·용매 1

HCID 7237O-Xylene용매

실험 절차

Ethyl propiolate (804 mg) was added to the o-xylene (15 mL) solution of tetrahydropyridino[1,2-c][1,2,3]oxadiazolone (1.04 g) under a nitrogen atmosphere and refluxed for 16 h. The solution was concentrated under a reduced pressure. The residue was applied to silica gel column chromatography, then the column was eluted with n-hexane-AcOEt (2/1-1/1). The titled compound was obtained as yellow oil (871 mg, 65%), and 4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine-3-carboxylic acid ethyl ester was obtained as yellow oil (345 mg, 26%).

후처리

  1. temperaturerefluxed for 16 h
  2. concentrationThe solution was concentrated under a reduced pressure
  3. washthe column was eluted with n-hexane-AcOEt (2/1-1/1)

출처 및 근거

ORD 기록
ord-4ee70bce93f14af8a09c2eb5e29e75d7
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07812014B2

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