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Ethyl cyanoacetate → HCID 13728611, 화합물

HRID 986756
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HRID 986756 반응식
[C:1]([C:4]1[CH:5]=[CH:6][C:7]2[O:12][CH:11]=[C:10]([C:13]#N)[C:9](=[O:15])[C:8]=2[CH:16]=1)(=[O:3])[CH3:2].[C:17]([CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21])#[N:18].[NH:25]1CCCCC1>C(O)C>[C:1]([C:4]1[CH:5]=[CH:6][C:7]2[O:12][C:11]3=[N:18][C:17]([NH2:25])=[C:19]([C:20]([O:22][CH2:23][CH3:24])=[O:21])[CH:13]=[C:10]3[C:9](=[O:15])[C:8]=2[CH:16]=1)(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7764Ethyl cyanoacetateHCID 8082PiperidineHCID 137286106-acetyl-4-oxo-4H-1-benzopyran-3-carbonitrile

생성물 1

HCID 13728611HCID 13728611, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

In ethanol (800 ml) was suspended 6-acetyl-4-oxo-4H-1-benzopyran-3-carbonitrile (32 g). To the suspension were added ethyl cyanoacetate (23.9 ml) and piperidine (23.7 ml). The mixture was refluxed for one hour, then cooled to room temperature. The resulting crystals were collected by filtration, washed with ethanol, then with acetone, followed by drying to give ethyl 7-acetyl-2-amino-5-oxo-5H-[1]benzopyrano[2,3-b]pyridine-3-carboxylate as yellow crystals (46.3 g). Melting point: >300° C.

후처리

  1. temperatureThe mixture was refluxed for one hour
  2. filtrationThe resulting crystals were collected by filtration
  3. washwashed with ethanol
  4. customby drying

출처 및 근거

ORD 기록
ord-8e835ff05a3c47818bffba484b806547
출처 데이터셋
uspto-grants-1987_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04716167

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