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Hydrochloric Acid → HCID 12763973, 화합물

HRID 1277965
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HRID 1277965 반응식
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[CH:8][C:9]3[N:10]2[CH:13]=[C:14]([C:16]([O:18]CC)=[O:17])[N:15]=3)=[CH:5][CH:4]=1.[OH-].[Na+].Cl>C(O)C>[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[CH:8][C:9]3[N:10]2[CH:13]=[C:14]([C:16]([OH:18])=[O:17])[N:15]=3)=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 12763974HCID 12763974, 화합물

생성물 1

HCID 12763973HCID 12763973, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

1.35 g of ethyl 8-methoxyimidazo-[1,2-a]-quinoline-2-carboxylate were dissolved in 60 ml of ethanol and 2.5 ml of 2 N sodium hydroxide were added thereto. The mixture was refluxed for 1 hour whereupon a colorless gel was produced and after 3 ml of 2 N hydrochloric acid were added, and the mixture was refluxed for another 60 minutes and then was allowed to cool to room temperature. The cream precipitate thus formed was filtered off and was recrystallized from glacial acetic acid and then was washed with methanol to obtain off-white crystals of 8-methoxyimidazo-[1,2-a]-quinoline-2-carboxylic acid melting at 272°-273° C.

후처리

  1. temperatureThe mixture was refluxed for 1 hour whereupon a colorless gel
  2. customwas produced
  3. temperaturethe mixture was refluxed for another 60 minutes
  4. customThe cream precipitate thus formed
  5. filtrationwas filtered off
  6. customwas recrystallized from glacial acetic acid
  7. washwas washed with methanol

출처 및 근거

ORD 기록
ord-6d3ef4f6ece64233b814eaf85da40dca
출처 데이터셋
uspto-grants-1981_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04279912

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