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Triethylamine → HCID 23447909、化合物

HRID 1840300
ノート
印刷プレビュー

反応式

HRID 1840300 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

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

生成物 1

HCID 23447909HCID 23447909、化合物収率 80.2%

試薬・触媒・溶媒 2

HCID 962Water
溶媒
HCID 6228Dimethylformamide溶媒

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-47e3b4f2a1a04753ad36ad04d5a8784f
出典データセット
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06680319B2

反応ノート

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