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Chloroform → Ethyl Acetate

HRID 433907
ノート
印刷プレビュー

反応式

HRID 433907 の反応式
C(N1[CH:12]=[CH:11]N=C1)(N1C=CN=C1)=O.[N:13]1([C:21]2[CH:29]=[CH:28][C:24]([C:25]([OH:27])=[O:26])=[CH:23][CH:22]=2)[CH2:19][CH2:18][C:17](=[O:20])[NH:16][CH2:15][CH2:14]1.[NH2:30][C@H:31]1[CH2:36][C:35]2[C:37]([N:41]3[CH2:46][CH2:45][N:44]([CH3:47])[CH2:43][CH2:42]3)=[CH:38][CH:39]=[CH:40][C:34]=2[O:33][CH2:32]1.C(Cl)(Cl)Cl>CN(C)C=O.C(O)C>[C:25]([O:27][CH2:11][CH3:12])(=[O:26])[CH3:24].[CH3:47][N:44]1[CH2:45][CH2:46][N:41]([C:37]2[C:35]3[CH2:36][C@H:31]([NH:30][C:25](=[O:27])[C:24]4[CH:23]=[CH:22][C:21]([N:13]5[CH2:19][CH2:18][C:17](=[O:20])[NH:16][CH2:15][CH2:14]5)=[CH:29][CH:28]=4)[CH2:32][O:33][C:34]=3[CH:40]=[CH:39][CH:38]=2)[CH2:42][CH2:43]1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 6212ChloroformHCID 682631,1'-CarbonyldiimidazoleHCID 11139461(S)-3-amino-5-(4-methylpiperazin-1-yl)-1,4-dihydro-2H-1-benzopyranHCID 220640304-(5-Oxo-1,4-diazepan-1-YL)benzoic acid

生成物 2

HCID 8857Ethyl Acetate収率 204.2%HCID 22896527HCID 22896527、化合物

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 6228Dimethylformamide溶媒2 回

実験手順

A solution of 1,1′-carbonyldiimidazole (151 mg, 0.934 mmol) and 4-(hexahydro-1,4-diazepin-5-on-1-yl)benzoic acid (219 mg, 0.934 mmol) in anhydrous N,N-dimethylformamide (7 mL) was stirred at 75° C. for 55 min. The mixture was allowed to cool, and a solution of (S)-3-amino-5-(4-methylpiperazin-1-yl)-3,4-dihydro-2H-1-benzopyran (210 mg, 0.85 mmol) in N,N-dimethylformamide (3.5 mL) was added. The reaction mixture was stirred at room temperature for 14 days. The solvent was removed in vacuo, and the residue was purified by column chromatography on silica (eluent: chloroform/ethanol, 90:10+1% conc. NH3). The product was crystallized from a mixture of chloroform, ethanol, and ethyl acetate affording 84 mg (21% yield) of the title compound as white crystals: mp 244-247° C. (decomposes); [α]21D−148° (c 0.50, chloroform); TSPMS (70 eV) m/z 464 (M+1).

後処理

  1. temperatureto cool
  2. customThe solvent was removed in vacuo
  3. customthe residue was purified by column chromatography on silica (eluent: chloroform/ethanol, 90:10+1% conc. NH3)

出典と根拠

ORDレコード
ord-051da950ade7454bbb99414e8201f9d6
出典データセット
uspto-grants-2003_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06670359B2

反応ノート

読み込み中…

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