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Ethyl bromopyruvate → HCID 12763970, 화합물

HRID 1277961
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HRID 1277961 반응식
[NH2:1][C:2]1[CH:11]=[C:10]([Cl:12])[C:9]2[C:4](=[CH:5][C:6]([O:13][CH3:14])=[CH:7][CH:8]=2)[N:3]=1.Br[CH2:16][C:17](=O)[C:18]([O:20][CH2:21][CH3:22])=[O:19]>C(COC)OC>[Cl:12][C:10]1[C:9]2[C:4](=[CH:5][C:6]([O:13][CH3:14])=[CH:7][CH:8]=2)[N:3]2[CH:16]=[C:17]([C:18]([O:20][CH2:21][CH3:22])=[O:19])[N:1]=[C:2]2[CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 66144Ethyl bromopyruvateHCID 14067409HCID 14067409, 화합물

생성물 1

HCID 12763970HCID 12763970, 화합물

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

실험 절차

1.3 g of 2-amino-4-chloro-7-methoxyquinoline were dissolved in 20 ml of dimethoxyethane and 1.3 g of ethyl bromopyruvate were added thereto. The mixture was stirred at room temperature for 2 hours and the crystalline intermediate thus formed was filtered off, washed with ether and then was dissolved in 20 ml of ethanol. The resultant solution was refluxed for 3 hours and ethyl 5-chloro-8-methoxyimidazo-[1,2-a]-quinoline-2-carboxylate melting at 215°-216° C. was isolated by the procedure of Example 9.

후처리

  1. customthe crystalline intermediate thus formed
  2. filtrationwas filtered off
  3. washwashed with ether
  4. dissolutionwas dissolved in 20 ml of ethanol
  5. temperatureThe resultant solution was refluxed for 3 hours

출처 및 근거

ORD 기록
ord-9548466e723e485da6095f09e84db62b
출처 데이터셋
uspto-grants-1981_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04279912

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