Dimethylformamide → 4-Amino-2-[1-(ethoxy-4-methoxyphenyl)-3-hydroxybutyl]isoindoline-1,3-dione

HRID 433291ノート

反応式

HRID 433291 の反応式
Cl.[NH2:2][CH:3]([C:8]1[CH:13]=[CH:12][C:11]([O:14][CH3:15])=[C:10](OCC)[CH:9]=1)[CH2:4][CH:5]([OH:7])[CH3:6].[NH2:19][C:20]1[CH:35]=[CH:34][CH:33]=[C:22]2[C:23](N(C(OCC)=O)[C:26](=[O:27])[C:21]=12)=[O:24].C(N([CH2:41][CH3:42])CC)C.CN(C)C=[O:46]>>[NH2:19][C:20]1[CH:35]=[CH:34][CH:33]=[C:22]2[C:21]=1[C:26](=[O:27])[N:2]([CH:3]([C:8]1[CH:9]=[CH:10][C:11]([O:14][CH3:15])=[CH:12][C:13]=1[O:46][CH2:41][CH3:42])[CH2:4][CH:5]([OH:7])[CH3:6])[C:23]2=[O:24]

参加物

5

反応条件

温度
85 °C

実験手順

A mixture of 4-amino-4-(3-ethoxy-4-methoxyphenyl)butan-2-ol hydrochloride (1.0 g, 3.63 mmol), 3-amino-N-ethoxycarbonylphthalimide (0.85 g, 3.63 mmol) and triethylamine (2.37 g, 3.63 mmol) in dimethylformamide (15 mL) was heated at 80-90° C. for 16 hours. The mixture was concentrated in vacuo and the residue was stirred with methylene chloride (10 mL). The mixture was filtered and the filtrate was concentrated and purified by chromatography (silica gel, methylene chloride:ethyl acetate 8:2) to give 4-amino-2-[1-(ethoxy-4-methoxyphenyl)-3-hydroxybutyl]isoindoline-1,3-dione as a white solid (0.72 g, 52%); 1H NMR (CDCl3) δ7.41-7.35 (m, 1H), 7.11-7.05 (m, 3H), 6.83-6.80 (m, 2H), 5.54-5.48 (dd, J=4.1 and 11.8 Hz, 1H), 5.22 (s, 2H), 4.10 (q, 2H), 3.85 (s, 3H), 3.77 (m, 1H), 2.88-2.77 (m, 1H), 2.07-1.00 (m, 1H), 1.67 (s, 1H), 1.45 (t, 3H), 1.27 (d, 3H).

後処理

  1. concentrationThe mixture was concentrated in vacuo
  2. filtrationThe mixture was filtered
  3. concentrationthe filtrate was concentrated
  4. custompurified by chromatography (silica gel, methylene chloride:ethyl acetate 8:2)

出典と根拠

ORDレコード
ord-2f667475554e489db83dbdcaca96525b
出典データセット
uspto-grants-2003_12
特許番号
US06667316B1

反応ノート

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