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tert-butyl N-(1-carbamothioylpiperidin-4-yl)carbamate → Ethyl 2-(4-aminopiperidin-1-yl)-4-[(2-methoxyethoxy)methyl]-1,3-thiazole-5-carboxylate hydrochloride

HRID 2233892
ノート
印刷プレビュー

反応式

HRID 2233892 の反応式
[NH2:1][C:2]([N:4]1[CH2:9][CH2:8][CH:7]([NH:10]C(=O)OC(C)(C)C)[CH2:6][CH2:5]1)=[S:3].[Cl:18][CH:19]([C:25](=O)[CH2:26][O:27][CH2:28][CH2:29][O:30][CH3:31])[C:20]([O:22][CH2:23][CH3:24])=[O:21]>CCO>[ClH:18].[NH2:10][CH:7]1[CH2:6][CH2:5][N:4]([C:2]2[S:3][C:19]([C:20]([O:22][CH2:23][CH3:24])=[O:21])=[C:25]([CH2:26][O:27][CH2:28][CH2:29][O:30][CH3:31])[N:1]=2)[CH2:9][CH2:8]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 59296117tert-butyl N-(1-carbamothioylpiperidin-4-yl)carbamate2 回HCID 86038328Ethyl 2-chloro-4-(2-methoxyethoxy)-3-oxobutanoate2 回

生成物 1

HCID 68579915Ethyl 2-(4-aminopiperidin-1-yl)-4-[(2-methoxyethoxy)methyl]-1,3-thiazole-5-carboxylate hydrochloride

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
90 °C

実験手順

tert-Butyl [1-(aminocarbonothioyl)piperidin-4-yl]carbamate (Intermediate 125, 400 mg) was dissolved in anhydrous EtOH (5 ml). Ethyl 2-chloro-4-(2-methoxyethoxy)-3-oxobutanoate (Intermediate 124, 368 mg) was added and the mixture was heated at 90° C. for 18 h. Partial removal of Boc group was detected. Solvent was removed in vacuo and the dried material was treated with 4 N HCl/dioxane for 2 h. Solvent was removed in vacuo to give a brown/yellow solid which was dried to afford the title compound which was used without further purification (508 mg).

後処理

  1. customPartial removal of Boc group
  2. customSolvent was removed in vacuo
  3. additionthe dried material was treated with 4 N HCl/dioxane for 2 h
  4. customSolvent was removed in vacuo
  5. customto give a brown/yellow solid which
  6. customwas dried

出典と根拠

ORDレコード
ord-61cbc8f42d5c4c0ba076f7bea15964eb
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07709503B2

反応ノート

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