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Dimethylformamide → HCID 86686878, 화합물

HRID 533110
노트
인쇄 미리보기

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HRID 533110 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([C:14]#[C:15][C:16]2[CH:21]=[C:20]([Br:22])[CH:19]=[CH:18][C:17]=2[OH:23])[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].CN(C)C=O>[Cu](I)I.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C(N(CC)CC)C>[C:1]([O:5][C:6]([N:8]1[CH2:9][CH2:10][CH:11]([C:14]2[O:23][C:17]3[CH:18]=[CH:19][C:20]([Br:22])=[CH:21][C:16]=3[CH:15]=2)[CH2:12][CH2:13]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
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참가 물질

6

반응물 2

HCID 6228DimethylformamideHCID 866868774-(5-Bromo-2-hydroxy-phenylethynyl)-piperidine-1-carboxylic acid tert-butyl ester

생성물 1

HCID 86686878HCID 86686878, 화합물

시약·촉매·용매 3

HCID 83717Copper iodide촉매HCID 178418476HCID 178418476, 화합물촉매
HCID 8471
Triethylamine
용매

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온도
55 °C

실험 절차

A mixture of 4-(5-bromo-2-hydroxy-phenylethynyl)-piperidine-1-carboxylic acid tert-butyl ester (70 mg), copper iodide (9 mg), N,N-dimethylformamide (1 mL), triethylamine (100 μL), and Pd(PPh3)2Cl2 (7 mg) is heated under an argon atmosphere to 55° C. for 0.5 h. The reaction mixture is diluted with ice water after cooling to room temperature and extracted with ethyl acetate. The combined extracts are dried over MgSO4 and concentrated in vacuo. The residue is chromatographed on silica gel (cyclohexane/ethyl acetate 80:20→50:50) to give the title compound. LC (method 2): tR=1.49 min; Mass spectrum (ESI+): m/z=380, 382 [M+H]+.

후처리

  1. temperatureafter cooling to room temperature
  2. extractionextracted with ethyl acetate
  3. dry with materialThe combined extracts are dried over MgSO4
  4. concentrationconcentrated in vacuo
  5. customThe residue is chromatographed on silica gel (cyclohexane/ethyl acetate 80:20→50:50)

출처 및 근거

ORD 기록
ord-06141d448c0446f8be625e6d0f70c464
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08853239B2

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