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Triethylamine → HCID 23447909, 화합물

HRID 1840300
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HRID 1840300 반응식
[CH2:1]([C:3]1[O:7][N:6]=[C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:4]=1[C:14]([OH:16])=O)[CH3:2].Cl.[Cl:18][CH2:19][CH2:20][CH2:21][NH2:22].C(P(=O)(OCC)OCC)#N.C(N(CC)CC)C>CN(C)C=O.O>[Cl:18][CH2:19][CH2:20][CH2:21][NH:22][C:14]([C:4]1[C:5]([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)=[N:6][O:7][C:3]=1[CH2:1][CH3:2])=[O:16]
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참가 물질

7

반응물 4

HCID 8471TriethylamineHCID 76257Diethyl cyanophosphonateHCID 114690951-Propanamine, 3-chloro-, hydrochlorideHCID 135451045-Ethyl-3-phenyl-1,2-oxazole-4-carboxylic acid

생성물 1

HCID 23447909HCID 23447909, 화합물수율 80.2%

시약·촉매·용매 2

HCID 962Water
용매
HCID 6228Dimethylformamide용매

실험 절차

A solution of 3.1 g of 5-ethyl-3-phenylisoxazole-4-carboxylic acid (prepared as described in J. Org. Chem. 1985, 50, 5660-5666), 2.94 g of 3-chloropropylamine hydrochloride, 2.62 mL of 92% diethyl cyanoposphonate and 4.38 mL of triethylamine in 50 mL of anhydrous dimethylformamide was stirred at room temperature for 3 hours, poured into 500 mL of water and extracted with ethyl acetate (2×200 mL). The combined organic layers were washed with water, dried (sodium sulphate) and the solvent was evaporated under vacuum. The crude was purified by flash chromatography (ethyl acetate-petroleum ether 3:7) to give 3.35 g (73%) of the title compound. M.p. 75-76° C.

후처리

  1. extractionextracted with ethyl acetate (2×200 mL)
  2. washThe combined organic layers were washed with water
  3. dry with materialdried (sodium sulphate)
  4. customthe solvent was evaporated under vacuum
  5. customThe crude was purified by flash chromatography (ethyl acetate-petroleum ether 3:7)

출처 및 근거

ORD 기록
ord-47e3b4f2a1a04753ad36ad04d5a8784f
출처 데이터셋
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06680319B2

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