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Trifluoroacetic acid → HCID 10565105, 화합물

HRID 729235
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HRID 729235 반응식
[C:1]([N:4]1[CH2:13][CH2:12][C:11]2[C:6](=[CH:7][C:8]([NH2:14])=[CH:9][CH:10]=2)[CH2:5]1)(=[O:3])[CH3:2].[F:15][C:16]([F:21])([F:20])[C:17](O)=[O:18].FC(F)(F)C(OC(=O)C(F)(F)F)=O>C(Cl)Cl>[C:1]([N:4]1[CH2:13][CH2:12][C:11]2[C:6](=[CH:7][C:8]([NH:14][C:17](=[O:18])[C:16]([F:21])([F:20])[F:15])=[CH:9][CH:10]=2)[CH2:5]1)(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6422Trifluoroacetic acidHCID 9845Trifluoroacetic anhydrideHCID 128113521-(7-Amino-3,4-dihydroisoquinolin-2(1H)-yl)ethan-1-one

생성물 1

HCID 10565105HCID 10565105, 화합물수율 94%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 14 (3.0 g, 17 mmol), trifluoroacetic acid (2 ml, 28 mmol) and trifluoroacetic anhydride (4 ml, 28 mmol) in CH2Cl2 is refluxed for 15 minutes, cooled, and the mixture is poured onto ice, extracted twice with CH2Cl2 and evaporated. The mixture is chromatographed on silica gel to give 4.5 g of compound 15 (94% yield). 1H NMR [300 MHz, (CD3)2SO], a 3:2 mixture of amide conformers doubling most signals, δ 11.24 (0.8H, s, NH), 11.21 (1.2H, s, NH), 7.55-7.40 (2H, m, H5.8), 7.22 (0.6H, s, H-6), 7.20 (0.4H, s, H-6), 4.64 (0.8H, s, ArCH2N), 4.57 (1.2H, s, ArCH2N), 3.65 (2H, t, ArCH2CH2N), 2.84 (1.2H, t, ArCH2CH2N), 2.73 (0.8H, t, ArCH2CH2N), 2.06 (1.2H, s, COCH3), 2.05 (1.8H, s COCH3).

후처리

  1. temperaturecooled
  2. additionthe mixture is poured onto ice
  3. extractionextracted twice with CH2Cl2
  4. customevaporated
  5. customThe mixture is chromatographed on silica gel

출처 및 근거

ORD 기록
ord-19f15aad123f41cfadea4680d0d2d908
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07582616B2

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