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Triethylamine → HCID 131736934, 화합물

HRID 56435
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HRID 56435 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.O=C1CCC(=O)N1[C:25]([O:27][CH2:28][CH2:29][Si:30]([CH3:33])([CH3:32])[CH3:31])=[O:26]>O1CCOCC1.O.C(OCC)(=O)C>[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:25](=[O:26])[O:27][CH2:28][CH2:29][Si:30]([CH3:33])([CH3:32])[CH3:31]
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참가 물질

7

반응물 3

HCID 8471TriethylamineHCID 120428161-Pyrrolidinecarboxylic acid, 2,5-dioxo-, 2-(trimethylsilyl)ethyl esterHCID 118036559(4R,5R)-5-Amino-2,2-dimethyloxan-4-ol

생성물 1

HCID 131736934HCID 131736934, 화합물수율 52%

시약·촉매·용매 3

HCID 962Water용매
HCID 8857
Ethyl Acetate
용매
HCID 312751,4-Dioxane용매

실험 절차

To a solution of (4R,5R)-5-amino-2,2-dimethyl-tetrahydro-2H-pyran-4-ol (550 mg, 2.40 mmol) and triethylamine (484 mg, 4.80 mmol) in dioxane (5 mL) and water (5 mL) was added 2-(trimethylsilyl)ethyl 2,5-dioxopyrrolidine-1-carboxylate (750 mg, 2.90 mmol) at room temperature. 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 concentrated, and the residue was purification by silica gel column with petroleum ether/ethyl acetate=4/1 to 1/1 to afford the title compound (360 mg, 52% for 2 steps) as a gray solid.

후처리

  1. washwashed with brine
  2. concentrationThe organic layer was concentrated
  3. custompurification by silica gel column with petroleum ether/ethyl acetate=4/1 to 1/1

출처 및 근거

ORD 기록
ord-05f855ef1a414262ba407faebaf3eb46
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09434700B2

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