Hydrochloric Acid → Ethyl 7-aminoquinoline-3-carboxylate

HRID 51971

반응식

HRID 51971 반응식
Cl.[CH2:2]([O:4][C:5]([C:7]1[CH:8]=[N:9][C:10]2[C:15]([CH:16]=1)=[CH:14][CH:13]=[C:12]([N:17]=C(C1C=CC=CC=1)C1C=CC=CC=1)[CH:11]=2)=[O:6])[CH3:3]>C(O)C>[CH2:2]([O:4][C:5]([C:7]1[CH:8]=[N:9][C:10]2[C:15]([CH:16]=1)=[CH:14][CH:13]=[C:12]([NH2:17])[CH:11]=2)=[O:6])[CH3:3]

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 102872307-(Benzhydrylidene-amino)-quinoline-3-carboxylic acid ethyl ester

생성물 1

HCID 9877801Ethyl 7-aminoquinoline-3-carboxylate수율 68.3%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Concentrated hydrochloric acid (1 mL, 2.5 volumes) was added to a solution of 7-(benzhydrylidene-amino)-quinoline-3-carboxylic acid ethyl ester (400 mg, 1.05 mmol, 1 equiv) in ethanol (4 mL, 10 volumes). The solution was stirred at room temperature for three hours and then concentrated. The residue was dissolved in ethyl acetate (20 mL, 50 volumes) and the organic layer was washed with 1 N hydrochloric acid (5×25 mL). The pH of the combined aqueous layer was then adjusted to about 8 with solid sodium hydroxide. The aqueous layer was then extracted with ethyl acetate (3×50 mL). The combined organic layers were dried over sodium sulfate and concentrated to provide 7-amino-quinoline-3-carboxylic acid ethyl ester (155 mg, 68%) as a yellow solid. The crude solid can be further purified by flash column chromatography using silica gel (EM Science, Gibbstown, N.J., 230-400 mesh) in 60% ethyl acetate in hexanes if desired.

후처리

  1. concentrationconcentrated
  2. dissolutionThe residue was dissolved in ethyl acetate (20 mL, 50 volumes)
  3. washthe organic layer was washed with 1 N hydrochloric acid (5×25 mL)
  4. extractionThe aqueous layer was then extracted with ethyl acetate (3×50 mL)
  5. dry with materialThe combined organic layers were dried over sodium sulfate
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-194726897d924469839c471fea67f027
출처 데이터셋
uspto-grants-2004_03
특허 번호
US06713489B2

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