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Acetonitrile → 3,5-Dimethyl-2-phenylethynyl-3H-imidazole-4-carboxylic acid ethyl ester

HRID 48940
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인쇄 미리보기

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HRID 48940 반응식
C(N(CC)CC)C.[C:8]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)#[CH:9].[CH2:16]([O:18][C:19]([C:21]1[N:22]([CH3:28])[C:23](Br)=[N:24][C:25]=1[CH3:26])=[O:20])[CH3:17].CC#N>CN(C=O)C.C(O)(C(F)(F)F)=O>[CH2:16]([O:18][C:19]([C:21]1[N:22]([CH3:28])[C:23]([C:9]#[C:8][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[N:24][C:25]=1[CH3:26])=[O:20])[CH3:17]
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참가 물질

7

반응물 4

HCID 6342AcetonitrileHCID 8471TriethylamineHCID 10821PhenylacetyleneHCID 13897513ethyl 2-bromo-1,4-dimethyl-1H-imidazole-5-carboxylate

생성물 1

HCID 98351263,5-Dimethyl-2-phenylethynyl-3H-imidazole-4-carboxylic acid ethyl ester수율 29%

시약·촉매·용매 2

HCID 6228
Dimethylformamide
용매
HCID 6422Trifluoroacetic acid용매

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온도
90 °C

실험 절차

In analogy to the method as described in Chem. Pharm. Bull. 1987, 35(2), 823-828, 17.5 mg (0.025 mmol) bis-(triphenylphosphine)-palladium-II-chloride, 2.9 mg (0.015 mmol) cuprous iodide, 60.5 mg (0.6 mmol) triethylamine, 32.4 mg (0.3 mmol) ethynylbenzene and 61.8 mg (0.25 mmol) 2-bromo-3,5-dimethyl-3H-imidazole-4-carboxylic acid ethyl ester are dissolved in 1 ml DMF and shaken for 3 h at 90° C. The title compound (19.3 mg, 29%, MS: m/e=269.3, [M+H+]) was isolated from the reaction mixture by HPLC chromatography (YMC CombiPrep C18 column 50×20 mm, solvent gradient 10-95% CH3CN in 0.1 % TFA(aq) over 6.0 min, λ=230 nm, flow rate 40 ml/min).

출처 및 근거

ORD 기록
ord-47219f08aa5c4ac497f38e43054e7af5
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06706707B2

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