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Triethylamine → HCID 131736938、化合物

HRID 56440
ノート
印刷プレビュー

反応式

HRID 56440 の反応式
[NH2:1][C@H:2]1[CH2:7][O:6][C:5]([CH3:9])([CH3:8])[CH2:4][C@@H:3]1[OH:10].C(N(CC)CC)C.O1CCOCC1.O=C1CCC(=O)N1[C:31]([O:33][CH2:34][CH2:35][Si:36]([CH3:39])([CH3:38])[CH3:37])=[O:32]>C(OCC)(=O)C.O>[OH:10][C@H:3]1[CH2:4][C:5]([CH3:9])([CH3:8])[O:6][CH2:7][C@@H:2]1[NH:1][C:31](=[O:32])[O:33][CH2:34][CH2:35][Si:36]([CH3:39])([CH3:38])[CH3:37]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 8471TriethylamineHCID 312751,4-DioxaneHCID 120428161-Pyrrolidinecarboxylic acid, 2,5-dioxo-, 2-(trimethylsilyl)ethyl esterHCID 118036455(4S,5S)-5-amino-2,2-dimethyl-tetrahydropyran-4-ol

生成物 1

HCID 131736938HCID 131736938、化合物収率 86.4%

試薬・触媒・溶媒 2

HCID 962
Water
溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of (4S,5S)-5-amino-2,2-dimethyl-tetrahydro-2H-pyran-4-ol (1.1 g, 4.0 mmol) and triethylamine (1.1 mL, 8.0 mmol) in a mixed solvent of dioxane (5 mL) and water (5 mL) at room temperature was added 2-(trimethylsilyl)ethyl 2,5-dioxopyrrolidine-1-carboxylate (1.2 g, 4.8 mmol). The reaction mixture was stirred at room temperature for 4 hours. After that, the solution was diluted with ethyl acetate and washed with brine. The organic layer was separated and concentrated. The resulting residue was purified by silica gel chromatography using petroleum ether/ethyl acetate=4/1 to 1/1 as the eluent to afford the title compound (1.0 g, 86% for 2 steps) as a yellow oil.

後処理

  1. washwashed with brine
  2. customThe organic layer was separated
  3. concentrationconcentrated
  4. customThe resulting residue was purified by silica gel chromatography

出典と根拠

ORDレコード
ord-fa1c4eb34b68477a85de154b8abe9262
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09434700B2

反応ノート

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