Methylamine → 4-Chloro-6-methyl-2-(4-methyl-piperazin-1-yl)-10,10-dioxo-10,11-dihydro-5-oxa-10lambda*6*-thia-dibenzo[a,d]cycloheptene-8-carboxylic acid
反応式
[CH3:1][NH2:2].C[O:4][C:5]([C:7]1[CH:8]=[C:9]([CH3:32])[C:10]2[O:16][C:15]3[C:17]([Cl:28])=[CH:18][C:19]([N:21]([CH2:25][CH2:26]Cl)[CH2:22][CH2:23]Cl)=[CH:20][C:14]=3[CH2:13][S:12](=[O:30])(=[O:29])[C:11]=2[CH:31]=1)=[O:6]>CO>[Cl:28][C:17]1[C:15]2[O:16][C:10]3[C:9]([CH3:32])=[CH:8][C:7]([C:5]([OH:4])=[O:6])=[CH:31][C:11]=3[S:12](=[O:29])(=[O:30])[CH2:13][C:14]=2[CH:20]=[C:19]([N:21]2[CH2:22][CH2:23][N:2]([CH3:1])[CH2:26][CH2:25]2)[CH:18]=1参加物
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
Methanolic methylamine solution (20% v/v, 6 mL) was added to a solution of Example 102 (0.330 g, 0.69 mmol) in methanol (2 mL) in an atmosphere of nitrogen and sealed in a pressure reactor vessel at 100° C. for 6 h. It was brought to room temperature, flushed with N2 gas, treated with chilled water and dilute HCl to neutral pH. The solid that precipitated was filtered, washed with water, dried and purified using flash chromatography (silica gel, MeOH/CHCl3) to obtain the title compound as an off white solid. Yield: 0.260 g (86.37%). 1H NMR (DMSO-d6): δ 2.40 (s, 3H, CH3), 2.70 (s, 3H, CH3), 2.72-2.75 (m, 4H, 2CH2), 3.30-3.35 (m, 4H, 2CH2), 5.10 (s, 2H, CH2), 7.10 (s, 1H, Ar), 7.20 (s, 1H, Ar), 8.10 (s, 1H, Ar) and 8.25 (s, 1H, Ar); MS: m/e (ES+) 436 (M+1).
後処理
- customsealed in a pressure reactor vessel at 100° C. for 6 h
- customwas brought to room temperature
- customflushed with N2 gas
- additiontreated with chilled water and dilute HCl to neutral pH
- customThe solid that precipitated
- filtrationwas filtered
- washwashed with water
- customdried
- custompurified
出典と根拠
- ORDレコード
- ord-f0ea493291a84ebcb9e00bca1285d7a3
- 出典データセット
- uspto-grants-2012_05
- 特許番号
- US08183234B2
反応ノート
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