Ethanolamine → HCID 19600242、化合物

HRID 611257ノート

反応式

HRID 611257 の反応式
[C:1]([C:9]1[CH:28]=[CH:27][C:12]([C:13]([N:15]2[CH2:20][CH2:19][C:18]3[CH:21]=[C:22]([C:24](O)=[O:25])[O:23][C:17]=3[CH2:16]2)=[O:14])=[CH:11][CH:10]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:29][CH2:30][CH2:31][OH:32].C(N(CC)CC)C.C(Cl)(Cl)(Cl)Cl.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[OH-].[Na+]>C(#N)C>[OH:32][CH2:31][CH2:30][NH:29][C:24]([C:22]1[O:23][C:17]2[CH2:16][N:15]([C:13](=[O:14])[C:12]3[CH:27]=[CH:28][C:9]([C:1](=[O:8])[C:2]4[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=4)=[CH:10][CH:11]=3)[CH2:20][CH2:19][C:18]=2[CH:21]=1)=[O:25]

参加物

8

実験手順

To a solution of 0.545 g (1.452 mmol) of 6-(4-benzoylbenzoyl)-4,5,6,7-tetrahydrofuro[2,3-c]pyridine-2-carboxylic acid, 98 mg (1.6 mmol) of 2-aminoethanol, 0.61 ml (4.4 mmol) of triethylamine and 1.40 ml (14.5 mmol) of carbon tetrachloride in 20 ml of acetonitrile, 1.14 g (4.36 mmol) of triphenylphosphine was added under ice-cooling, followed by stirring at room temperature for 4 hours. The reaction mixture was poured into aqueous sodium hydroxide and extracted with ethyl acetate 3 times. The combined organic layer was dried over anhydrous magnesium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (ethyl acetate to ethyl acetate/methanol=9/1); the resulting solid was washed with diethyl ether to yield the desired product.

後処理

  1. temperaturecooling
  2. extractionextracted with ethyl acetate 3 times
  3. dry with materialThe combined organic layer was dried over anhydrous magnesium sulfate
  4. distillationthe solvent was distilled off under reduced pressure
  5. customThe resulting crude product was purified by silica gel column chromatography (ethyl acetate to ethyl acetate/methanol=9/1)
  6. washthe resulting solid was washed with diethyl ether

出典と根拠

ORDレコード
ord-0fde3147b70742288e94cc35008d1e5d
出典データセット
uspto-grants-1999_12
特許番号
US05998433

反応ノート

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