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HCID 58505549、化合物 → HCID 178471307、化合物

HRID 1917600
ノート
印刷プレビュー

反応式

HRID 1917600 の反応式
C([O:8][C:9]1[CH:10]=[CH:11][N:12]2[C:16]([CH:17]=1)=[C:15]([C:18](=[O:23])[C:19]([CH3:22])([CH3:21])[CH3:20])[C:14]([CH2:24][C:25]([CH3:32])([CH3:31])[C:26]([O:28][CH2:29][CH3:30])=[O:27])=[C:13]2[C:33]([C:35]1[CH:40]=[CH:39][C:38]([Cl:41])=[CH:37][CH:36]=1)=[O:34])C1C=CC=CC=1>CCO.[Pd]>[Cl:41][C:38]1[CH:37]=[CH:36][C:35]([C:33]([C:13]2[N:12]3[C:16]([CH:17]=[C:9]([OH:8])[CH:10]=[CH:11]3)=[C:15]([C:18](=[O:23])[C:19]([CH3:21])([CH3:22])[CH3:20])[C:14]=2[CH2:24][C:25]([CH3:31])([CH3:32])[C:26]([O:28][CH2:29][CH3:30])=[O:27])=[O:34])=[CH:40][CH:39]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 58505549HCID 58505549、化合物

生成物 1

HCID 178471307HCID 178471307、化合物収率 85%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

To a stirred solution of ethyl 3-[7-(benzyloxy)-3-[(4-chlorophenyl)carbonyl]-1-(2,2-dimethylpropanoyl)indolizin-2-yl]-2,2-dimethylpropanoate (3.50 g, 6.10 mmol) in EtOH (50 mL) is added 10% Pd/C (480 mg). The suspension is stirred under an atmosphere of hydrogen for 1.5 h then filtered through a pad of diatomaceous earth and washed with EtOH. The filtrate is concentrated in vacuo to give ethyl 3-{3-[(4-chlorophenyl)carbonyl]-1-(2,2-dimethylpropanoyl)-7-hydroxyindolizin-2-yl}-2,2-dimethylpropanoate (2.50 g, 85%). Also obtained is ethyl 3-[1-(2,2-dimethylpropanoyl)-7-hydroxy-3-(phenylcarbonyl)indolizin-2-yl]-2,2-dimethylpropanoate (0.28 g, 10%). A suspension of ethyl 3-{3-[(4-chlorophenyl)carbonyl]-1-(2,2-dimethylpropanoyl)-7-hydroxyindolizin-2-yl}-2,2-dimethylpropanoate (100 mg, 0.207 mmol), 2-(chloromethyl)quinoline-HCl (66.0 mg, 0.310 mmol), and potassium carbonate (114 mg, 0.826 mmol) in DMF (3 mL) is stirred for 24 h at 23° C. The mixture is filtered and concentrated in vacuo to give ethyl 3-{3-[(4-chlorophenyl)carbonyl]-1-(2,2-dimethylpropanoyl)-7-(quinolin-2-ylmethoxy)indolizin-2-yl}-2,2-dimethylpropanoate that is dissolved in THF (2 mL), MeOH (3 mL), and 6M aqueous NaOH (2 mL) and heated at 70° C. for 1 h then cooled to 23° C. and acidified to pH=1 with concentrated aqueous HCl. The mixture is partitioned between CH2Cl2 and brine then organics are dried with MgSO4, filtered, and concentrated in vacuo. Purification of the crude by HPLC (25 to 75% CH3CN/0.1% TFA in water) gives the title compound (60 mg, 49%).

後処理

  1. filtrationthen filtered through a pad of diatomaceous earth
  2. washwashed with EtOH
  3. concentrationThe filtrate is concentrated in vacuo

出典と根拠

ORDレコード
ord-fa691808fcdd4106ba956c66d3e14667
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08618300B2

反応ノート

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