Pentanenitrile, 4,4-dimethyl-3-oxo- → HCID 66644209、化合物

HRID 1931074ノート

反応式

HRID 1931074 の反応式
[ClH:1].Cl.[CH:3]1([CH2:6][NH:7][NH2:8])[CH2:5][CH2:4]1.[CH3:9][C:10]([CH3:17])([CH3:16])[C:11](=O)[CH2:12][C:13]#[N:14]>C(O)C>[ClH:1].[C:10]([C:11]1[CH:12]=[C:13]([NH2:14])[N:7]([CH2:6][CH:3]2[CH2:5][CH2:4]2)[N:8]=1)([CH3:17])([CH3:16])[CH3:9]

参加物

4

反応物 2

HCID 108871Pentanenitrile, 4,4-dimethyl-3-oxo-HCID 43810474(Cyclopropylmethyl)hydrazine--hydrogen chloride (1/2)

生成物 1

HCID 66644209HCID 66644209、化合物収率 90%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A mixture of Example 27B (13.5 g, 85 mmol) and 4,4-dimethyl-3-oxopentanenitrile (11.69 g, 93 mmol) in ethanol (50 mL) was refluxed at 90° C. for 6 hours. The mixture was concentrated under reduced pressure and ethyl acetate (20mL) added to the residue. The white solid precipitate was filtered, washed with ether and dried to yield 17.5 g (90%) of title compound as a white solid. 1H NMR (300 MHz, DMSO-d6) δ ppm 0.42-0.54 (m, 4H), 1.16-1.27 (m, 1H), 1.28 (s, 9H), 4.02 (d, J=7.12 Hz, 2H), 5.53 (s, 1H), 6.91 (s, 2H), 14.05 (s, 1H); H); MS (DCI) m/z 294 [M+H]+.

後処理

  1. concentrationThe mixture was concentrated under reduced pressure and ethyl acetate (20mL)
  2. additionadded to the residue
  3. filtrationThe white solid precipitate was filtered
  4. washwashed with ether
  5. customdried

出典と根拠

ORDレコード
ord-faa7c7aae34f41c591ecad2d8457dae1
出典データセット
uspto-grants-2012_05
特許番号
US08188135B2

反応ノート

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