Hydrochloric Acid → 3-Methyl-5-phenyl-1,3-dihydro-benzo[e][1,4]diazepin-2-one

HRID 1435805

Reaktionsgleichung

Reaktionsgleichung von HRID 1435805
C(OC(=O)[NH:7][CH:8]([C:10](=[O:26])[NH:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[C:18](=O)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[CH3:9])(C)(C)C.Cl>C(Cl)(Cl)Cl>[CH3:9][CH:8]1[C:10](=[O:26])[NH:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[C:18]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[N:7]1

Komponenten

4

Edukt 2

HCID 313Hydrochloric AcidHCID 68524295[1-(2-Benzoyl-phenylcarbamoyl)-ethyl]-carbamic acid tert-butyl ester

Produkt 1

HCID 110322973-Methyl-5-phenyl-1,3-dihydro-benzo[e][1,4]diazepin-2-oneAusbeute 83 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6212ChloroformLösungsmittel

Versuchsvorschrift

To a stirred solution of the benzophenone 109 (10.65 g, 29.38 mmol) in CHCl3 (400 mL) at rt, hydrogen chloride gas was added in slowly. After 20 min, the addition was stopped and the solution was stirred overnight at rt. The reaction mixture was washed with a saturated solution of sodium bicarbonate (2×50 mL) and water (2×50 mL). The organic layer was concentrated under reduced pressure. The residual oil was dissolved in methanol-water (2:1, 500 mL) and the pH was adjusted to 8.5 by the addition of aqueous sodium hydroxide (1 N). The reaction mixture was stirred for 10 h at rt. The solution was concentrated under reduced pressure and water (100 mL) was added. The solution was extracted with CH2Cl2 (3×100 mL) and concentrated under reduced pressure. The crude solid 110 was purified by recrystallization from methanol/water to provide 110 (6.10 g, 83%). mp 160-162° C.; IR (KBr, cm−1) 3215, 3059, 2974, 2932, 1681, 1574, 1478, 1445, 1372, 1321, 1242, 1160, 1131; 1H NMR (CDCl3) δ 9.65 (s, 1H), 7.54-7.13 (m, 9H), 3.78 (q, J=6.5 Hz, 1H), 1.78 (d, J=7.1 Hz, 3H); MS (EI) m/e (relative intensity) 250 (M+, 40), 249 (83), 234 (15), 209 (75), 208 (76), 207 (100), 180 (17), 152 (19) 103 (23), 77 (40); [α]26D=290.2 (c 0.78, EtOAc).

Aufarbeitung

  1. additionthe addition
  2. washThe reaction mixture was washed with a saturated solution of sodium bicarbonate (2×50 mL) and water (2×50 mL)
  3. concentrationThe organic layer was concentrated under reduced pressure
  4. dissolutionThe residual oil was dissolved in methanol-water (2:1, 500 mL)
  5. additionthe pH was adjusted to 8.5 by the addition of aqueous sodium hydroxide (1 N)
  6. stirringThe reaction mixture was stirred for 10 h at rt
  7. concentrationThe solution was concentrated under reduced pressure and water (100 mL)
  8. additionwas added
  9. extractionThe solution was extracted with CH2Cl2 (3×100 mL)
  10. concentrationconcentrated under reduced pressure
  11. customThe crude solid 110 was purified by recrystallization from methanol/water

Quellen und Nachweise

ORD-Eintrag
ord-4e2a40d5bef04af19ce3b9520bbc963c
Quelldatensatz
uspto-grants-2009_11
Patentnummer
US07618958B2

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