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Methylamine → N2-Ethoxymethyl-N4-(4-methoxy-phenyl)-N2,N4-dimethyl-quinazoline-2,4-diamine

HRID 1876151
ノート
印刷プレビュー

反応式

HRID 1876151 の反応式
Cl.Cl[C:3]1[N:12]=[C:11]([N:13]([C:15]2[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=2)[CH3:14])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:4]=1.[CH3:23][NH2:24].[C:25]([O:28][CH2:29]C)(=O)[CH3:26]>CC(O)C.O>[CH2:25]([O:28][CH2:29][N:24]([CH3:23])[C:3]1[N:12]=[C:11]([N:13]([C:15]2[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=2)[CH3:14])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:4]=1)[CH3:26]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 6329MethylamineHCID 8857Ethyl AcetateHCID 86639964(2-Chloroquinazolin-4-yl)-(4-methoxyphenyl)-methylamine hydrochloride

生成物 1

HCID 59242060N2-Ethoxymethyl-N4-(4-methoxy-phenyl)-N2,N4-dimethyl-quinazoline-2,4-diamine収率 72%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 3776
Isopropanol
溶媒

反応条件

温度
100 °C

実験手順

To a solution of (2-chloroquinazolin-4-yl)-(4-methoxyphenyl)-methylamine hydrochloride (0.50 g, 1.50 mmol) in 10 mL of 2-propanol was added 2.0 M solution of methylamine (3.0 mL). The mixture was heated at 100° C. overnight with stirring. The solution was diluted with 20 mL of water and 50 mL of ethyl acetate. The organic layer was washed with water, then dried and concentrated. The resulting material was dissolved in 8 mL of ethanol and then 0.22 mL of formaldehyde (37% in water), a few drops of 5% sodium hydroxide solution were added. The mixture was heated at 90° C. for 1 d with stirring, and then diluted with 10 mL of water and 30 mL of ethyl acetate. The organic layer was washed with water, then dried and concentrated. The resulting crude material was purified by silica gel column chromatography to give the title compound (0.38 mg, 72%). 1H NMR (CDCl3, 400 MHz) δ 7.22 (d, 1H, J=8.4 Hz), 7.18 (t, 1H, J=6.8 Hz), 7.09 (d, 2H, J=8.8 Hz), 6.98 (d, 2H, J=8.8 Hz), 6.92 (d, 1H, J=8.4 Hz), 6.67 (t, 1H, J=6.8 Hz), 5.30 (s, 2H), 3.90 (s, 3H), 3.57 (q, 2H, J=6.8 Hz), 3.49 (s, 3H), 3.22 (s, 3H), 1.17 (t, 3H, J=6.8 Hz); ESI-MS m/z 353 (M+H)+.

後処理

  1. washThe organic layer was washed with water
  2. customdried
  3. concentrationconcentrated
  4. dissolutionThe resulting material was dissolved in 8 mL of ethanol
  5. addition0.22 mL of formaldehyde (37% in water), a few drops of 5% sodium hydroxide solution were added
  6. temperatureThe mixture was heated at 90° C. for 1 d
  7. stirringwith stirring
  8. additiondiluted with 10 mL of water and 30 mL of ethyl acetate
  9. washThe organic layer was washed with water
  10. customdried
  11. concentrationconcentrated
  12. customThe resulting crude material was purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-ec19be825890422d85717bc66627dc0e
出典データセット
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08309562B2

反応ノート

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