تفاعل #93041

ord-a5f7d684d7404733a8d26192b2d7931d

معادلة التفاعل

N[C@@H]1C(=O)N2C(C(=O)OCc3ccccc3)CS[C@H]12
Benzyl 6β-aminopenam-3-carboxylate
COC(OC)OC
trimethylorthoformate
O=Cc1ccc([N+](=O)[O-])cc1
4-nitrobenzaldehyde
O=C(OCc1ccccc1)C1CS[C@@H]2[C@H](N=Cc3ccc([N+](=O)[O-])cc3)C(=O)N12
Benzyl 6β-(4-nitrobenzylideneamino)penam-3-caboxylate

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe mixture was then evaporated to dryness
  2. 2
    أخرىtriturated with ethanol
  3. 3
    ترشيحthe solid material collected by filtration
  4. 4
    أخرىRenystallisation from ethanol/ethylacetate gave almost colourless needles (1.2 g 74%)

الإجراء التجريبي

Benzyl 6β-aminopenam-3-carboxylate (1.11 g, 4 m mol) in dry dichloromethane (4ml) with trimethylorthoformate (0.42 g, 0.44 ml, 4 m mol) was treated with 4-nitrobenzaldehyde (0.61 g, 0.4 m mol) in dry methanol (10 ml) at room temperature for 1.5 h. The mixture was then evaporated to dryness, triturated with ethanol and the solid material collected by filtration. Renystallisation from ethanol/ethylacetate gave almost colourless needles (1.2 g 74%); m.p. 95-96 C; νmax (CH2Cl2) 1795, 1750, 1530, 1360 cm-1 ; δ(CDCl3) 8.68 (1H, d, J 2Hz, CH=N), 8.27 and 7.94 (4H, 2d, J 9Hz, nitrophenyl), 7.38 (5H, s, phenyl), 5.51 (1H, d, J 4Hz, 5-H), 5.45 (1H, dd, J 2Hz and 4 Hz, 6-H), 5.23 (2H, s, CH2Ph), 4.93 (1H, t, J 5.5Hz, 3-H) and 3.45 (2H, d, J 5.5H±, 2-H)

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04609652uspto-grants-1986_09