Tetrahydrofuran → HCID 86632863, 화합물

HRID 1398750노트

반응식

HRID 1398750 반응식
Cl.[CH2:2]([O:4][C:5](=[O:9])[CH2:6][CH2:7][NH2:8])[CH3:3].Cl[C:11]1[C:16]([N+:17]([O-:19])=[O:18])=[CH:15][CH:14]=[CH:13][C:12]=1[N+:20]([O-:22])=[O:21].C(N(CC)CC)C.O1CCCC1>C(OCC)(=O)C>[N+:17]([C:16]1[CH:15]=[CH:14][CH:13]=[C:12]([N+:20]([O-:22])=[O:21])[C:11]=1[NH:8][CH2:7][CH2:6][C:5]([O:4][CH2:2][CH3:3])=[O:9])([O-:19])=[O:18]

참가 물질

6

반응물 4

HCID 8028TetrahydrofuranHCID 8471Triethylamine2회HCID 118141-Chloro-2,6-dinitrobenzeneHCID 458475beta-Alanine, ethyl ester, hydrochloride2회

생성물 1

HCID 86632863HCID 86632863, 화합물수율 99.6%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

A mixture of beta-alanine ethyl ester hydrochloride (911 mg, 5.39 mmol), 2-chloro-1,3-dinitrobenzene (1.00 g, 4.94 mmol), triethylamine (2.07 mL, 14.9 mmol) and tetrahydrofuran (50 mL) was stirred at room temperature for 2 hr. To the reaction mixture were added beta-alanine ethyl ester hydrochloride (455 mg, 2.96 mmol) and triethylamine (1.03 mL, 7.39 mmol) at room temperature and the resultant mixture was stirred at room temperature for 2 hr. The reaction mixture was diluted with ethyl acetate, washed with water and brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash column chromatography on, silica gel eluting with a 0-20% ethyl acetate/n-hexane gradient mixture to give the title compound as an oil (1.39 g, 4.92 mmol, 99.6%).

후처리

  1. washwashed with water and brine
  2. dry with materialdried over anhydrous sodium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by flash column chromatography on, silica gel eluting with a 0-20% ethyl acetate/n-hexane gradient mixture

출처 및 근거

ORD 기록
ord-1fe179fd8797437e8cad83b104b91633
출처 데이터셋
uspto-grants-2014_12
특허 번호
US08901141B2

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