1,4-Dioxane → HCID 70632848, compound

HRID 1415412Notes

Reaction equation

HRID 1415412 reaction equation
[C:1]1(=[O:24])[N:5]([CH:6]2[C:17](=[O:18])[N:8]3[C:9]([C:14]([OH:16])=[O:15])=[C:10]([CH3:13])[CH2:11][S:12][C@H:7]23)[C:4](=[O:19])[C:3]2=[CH:20][CH:21]=[CH:22][CH:23]=[C:2]12.O1[CH2:30][CH2:29][O:28][CH2:27]C1>O>[C:4]1(=[O:19])[N:5]([CH:6]2[C:17](=[O:18])[N:8]3[C:9]([C:14]([O:16][CH2:3][C:2]4[CH:1]=[CH:30][C:29]([O:28][CH3:27])=[CH:22][CH:23]=4)=[O:15])=[C:10]([CH3:13])[CH2:11][S:12][C@H:7]23)[C:1](=[O:24])[C:2]2=[CH:23][CH:22]=[CH:21][CH:20]=[C:3]12

Participants

4

Reactant 2

HCID 312751,4-DioxaneHCID 70474055HCID 70474055, compound

Product 1

HCID 70632848HCID 70632848, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

To a suspension of 13.4 g. (38 mmol.) of 7-phthalimido-3-methyl-3 -cephem-4-carboxylic acid in 20 ml. of dioxane and 10 ml. of water were slowly added 3.8 g. of KHCO3. The solution was evaporated to dryness, and 100 ml. of DMF and 8.8 g. of p-methoxybenzyl bromide were added to the potassium salt residue. The mixture was stirred for 2 hrs. and then poured onto 200 g. of ice. The resulting mixture was extracted twice with ethyl acetate. The extract was washed with water and brine, dried, and the solvent was then evaporated. The residue was recrystallized from ethyl acetate. Yield: 4.1 g. of large crystals, m.p. 118°-121°; second crop 1.8 g.; [α]D + 41.2° (MeCN), ir (CHCl3) 1800, 1785, 1745 and 1735 cm-1, nmr (CDCl3) δ 2.15 (s, 3, CH3); 3.0 and 3.7 (ABq, 2, J = 15 Hz), 3.8 (s, 3, CH3), 5.11 (d, 1, J = 4.5 Hz), 5.28 (s, 2, CH2), 5.75 (d, 1, J = 4.5 Hz), 6.8-7.8 (m, 8).

Workup

  1. additionTo a suspension of 13.4 g
  2. customThe solution was evaporated to dryness, and 100 ml
  3. additionof p-methoxybenzyl bromide were added to the potassium salt residue
  4. additionand then poured onto 200 g
  5. extractionThe resulting mixture was extracted twice with ethyl acetate
  6. washThe extract was washed with water and brine
  7. customdried
  8. customthe solvent was then evaporated
  9. customThe residue was recrystallized from ethyl acetate
  10. custom[α]D + 41.2° (MeCN), ir (CHCl3) 1800, 1785, 1745 and 1735 cm-1, nmr (CDCl3) δ 2.15 (s, 3, CH3); 3.0 and 3.7 (ABq, 2, J = 15 Hz), 3.8 (s, 3, CH3), 5.11 (d, 1, J = 4.5 Hz), 5.28 (s, 2, CH2), 5.75 (d, 1, J = 4.5 Hz), 6.8-7.8 (m, 8)

Sources & evidence

ORD record
ord-0ece1a43690f4ceaa4f6fb7076290744
Source dataset
uspto-grants-1977_01
Patent number
US04005074

Reaction notes

Loading…