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Hydrochloric Acid → HCID 67442213、化合物

HRID 1666605
ノート
印刷プレビュー

反応式

HRID 1666605 の反応式
NN1CCCC1.[Cl:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][C:15]([N:17]2[CH2:21][CH2:20][C@H:19]([NH:22][C:23]3[N:32]=[C:31]([N:33]4[CH2:38][CH2:37][N:36](C(OC(C)(C)C)=O)[CH2:35][CH2:34]4)[C:30]4[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=4)[N:24]=3)[CH2:18]2)=[O:16])=[CH:10][CH:9]=1.[ClH:46]>CO.C(OCC)(=O)C>[ClH:7].[ClH:46].[Cl:7][C:8]1[CH:9]=[CH:10][C:11]([CH2:14][C:15]([N:17]2[CH2:21][CH2:20][C@H:19]([NH:22][C:23]3[N:32]=[C:31]([N:33]4[CH2:38][CH2:37][NH:36][CH2:35][CH2:34]4)[C:30]4[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=4)[N:24]=3)[CH2:18]2)=[O:16])=[CH:12][CH:13]=1
参加物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 313Hydrochloric AcidHCID 279461-PyrrolidinamineHCID 57970094HCID 57970094、化合物

生成物 1

HCID 67442213HCID 67442213、化合物

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 8857Ethyl Acetate溶媒

実験手順

To a mixture of t-butyl 4-(2-((S)-pyrrolidin-3-ylamino)quinazolin-4-yl)piperazine-1-carboxylate (0.30 g), p-chlorophenylacetic acid (0.13 g), and chloroform (5 mL) were added HOBt.H2O (0.18 g) and EDC.HCl (0.18 g), and the mixture was stirred at room temperature for 2 days. To the reaction mixture was added saturated aqueous sodium hydrogencarbonate, and the mixture was extracted with chloroform. The organic layer was dried with anhydrous sodium sulfate, the desiccant was removed by filtration, the filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (NH silica gel, hexane/ethyl acetate=3:2) to obtain t-butyl 4-(2-((S)-1-(2-(4-chlorophenyl)ethanoyl)pyrrolidin-3-ylamino)quinazolin-4-yl)piperazine-1-carboxylate (0.29 g). (2) To a solution of t-butyl 4-(2-((S)-1-(2-(4-chlorophenyl)ethanoyl)pyrrolidin-3-ylamino)quinazolin-4-yl)piperazine-1-carboxylate (0.28 g) in methanol (5 mL) was added a solution (1.3 mL) of 4 M HCl in ethyl acetate, and the mixture was stirred overnight. The solvent was evaporated under reduced pressure, and the residue was crystallized in diethyl ether to obtain the title compound (0.15 g).

後処理

  1. customThe solvent was evaporated under reduced pressure
  2. customthe residue was crystallized in diethyl ether

出典と根拠

ORDレコード
ord-b284ae83416c482980bf0ad33bf6839c
出典データセット
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08044068B2

反応ノート

読み込み中…

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