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Borane;2-methylpropan-2-amine → ethyl 5,6-dihydro-4H-thieno[2,3-c]azepine-7(8H)-carboxylate

HRID 446724
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 446724
B.C(N)(C)(C)C.[Cl-].[Cl-].[Cl-].[Al+3].O=[C:12]1[CH2:18][CH2:17][N:16]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[CH2:15][C:14]2[S:24][CH:25]=[CH:26][C:13]1=2>C(Cl)Cl>[S:24]1[C:14]2[CH2:15][N:16]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[CH2:17][CH2:18][CH2:12][C:13]=2[CH:26]=[CH:25]1
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Komponenten

5

Edukt 3

HCID 517393Borane;2-methylpropan-2-amineHCID 6451240Aluminum(III) ChlorideHCID 13600418ethyl 4-oxo-5,6-dihydro-4H-thieno[2,3-c]azepine-7(8H)-carboxylate

Produkt 1

HCID 58293757ethyl 5,6-dihydro-4H-thieno[2,3-c]azepine-7(8H)-carboxylate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

Solid borane-t-butylamine pellets (2.77 g, 31.84 mmol) were crushed and suspended in methylene chloride (300 mL) at 0° C. Solid aluminum trichloride (2.12 g, 15.92 mmol) was added and the mixture was stirred for 1 hour. Compound 1043 (1.27 g, 5.31 mmol) was added slowly and the reaction mixture allowed to warm to room temperature overnight. The reaction was quenched by addition of ethanol (50 mL) then saturated ammonium chloride (100 mL). The mixture was brought to a neutral pH with saturated sodium bicarbonate, extracted with ethyl acetate (3×100 mL), and concentrated to give ethyl 5,6-dihydro-4H-thieno[2,3-c]azepine-7(8H)-carboxylate (Compound 1044) as a tan oil; 1H NMR (300 MHz, CDCl3): δ 6.95-6.85 (m, 1H), 6.70 (d, J=4.7 Hz, 1H), 4.49 (s, 2H), 4.18-4.00 (m, 2H), 3.66-3.58 (m, 2H), 2.77 (t, J=5.7 Hz, 2H), 1.62 (qn, J=6.0 Hz, 2H) and 1.24-1.08 (m, 3H).

Aufarbeitung

  1. customThe reaction was quenched by addition of ethanol (50 mL)
  2. extractionextracted with ethyl acetate (3×100 mL)
  3. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-00400f90ba3a4eb499348ac46ba752ee
Quelldatensatz
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08481524B2

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