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Triethylamine → Diisopropylether ethyl acetate

HRID 427342
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HRID 427342 반응식
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:10]([N+:13]([O-:15])=[O:14])=[C:9]2[C:4]=1[CH2:5][CH2:6][CH:7]([C:16]([OH:18])=[O:17])[CH2:8]2.S(Cl)(Cl)=O.[NH2:23][C:24]1[CH:37]=[CH:36][C:27]([C:28]([N:30]2[CH2:35][CH2:34][O:33][CH2:32][CH2:31]2)=[O:29])=[CH:26][CH:25]=1.[CH2:38](N([CH2:43][CH3:44])CC)[CH3:39]>CN(C)C=O.C(Cl)Cl.O.C1(C)C=CC=CC=1>[CH:3]([O:2][CH:43]([CH3:44])[CH3:24])([CH3:12])[CH3:4].[C:16]([O:18][CH2:38][CH3:39])(=[O:17])[CH3:7].[O:33]1[CH2:32][CH2:31][N:30]([C:28]([C:27]2[CH:36]=[CH:37][C:24]([NH:23][C:16]([CH:7]3[CH2:6][CH2:5][C:4]4[C:9](=[C:10]([N+:13]([O-:15])=[O:14])[CH:11]=[CH:12][C:3]=4[O:2][CH3:1])[CH2:8]3)=[O:18])=[CH:25][CH:26]=2)=[O:29])[CH2:35][CH2:34]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

10

반응물 4

HCID 8471TriethylamineHCID 24386Thionyl ChlorideHCID 5778154-(Morpholine-4-carbonyl)anilineHCID 186225095-Methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid

생성물 2

HCID 18622500N-(4-Morpholinocarbonylphenyl)-5-methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxamide
HCID 22281796
Diisopropylether ethyl acetate
수율 315.3%

시약·촉매·용매 4

HCID 6228Dimethylformamide촉매HCID 962Water용매HCID 1140Toluene용매HCID 6344Dichloromethane용매

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온도
60 °C

실험 절차

A mixture of 5-methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid (1.0 g, 4 mmol), toluene (20 mL), N,N-dimethylformamide (10 drops) and thionyl chloride (1.5 mL, 20 mmol) was heated at 60° C. for 1 h. The solvents were removed in vacuo and the residue, dissolved in methylene chloride (20 mL), was added to a solution of 4-aminobenzoylmorpholine (820 mg, 4 mmol, described in: Deylin J. P. J. Chem. Soc. Perkin Trans I, 1975, 830-841) and triethylamine (800 mg, 8 mmol) in methylene chloride (30 mL) at 5° C. After stirring at 20° C. for 2 h, water was added and the organic phase was separated, dried and the solvent removed in vacuo. The oily residue was crystallized from diisopropyl ether/ethyl acetate affording 1.2 g (73% yield) of the title compound as crystals: mp 186-189° C.; EIMS (70 eV) m/z (relative intensity) 439 (20, M+).

후처리

  1. customThe solvents were removed in vacuo
  2. dissolutionthe residue, dissolved in methylene chloride (20 mL)
  3. customthe organic phase was separated
  4. customdried
  5. customthe solvent removed in vacuo

출처 및 근거

ORD 기록
ord-717ba65c41b6443da0555ea0645bbe72
출처 데이터셋
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06313118B1

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