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Triethylamine → HCID 131736938, 화합물

HRID 56440
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HRID 56440 반응식
[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]
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참가 물질

7

반응물 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

생성물 1

HCID 131736938HCID 131736938, 화합물수율 86.4%

시약·촉매·용매 2

HCID 962
Water
용매
HCID 8857Ethyl Acetate용매

실험 절차

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.

후처리

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

출처 및 근거

ORD 기록
ord-fa1c4eb34b68477a85de154b8abe9262
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09434700B2

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