反応 #451707

反応方程式

p-nitrobenzyl 7-{2-(2-formamido-4-thiazolyl)-2-methoxyiminoacetamido}-3-chloro-3-cephem-4-carboxylate

→

7-{2-(2-formamido-4-thiazolyl)-2-methoxyiminoacetamido}-3-chloro-3-cephem-4-carboxylic acid

収率 52.8%

溶媒

methanol

tetrahydrofuran

反応条件

後処理

1. 1
   その他After removing the catalyst from the reaction mixture
2. 2
   濃縮the filtrate was concentrated under reduced pressure
3. 3
   workup.ADDITIONWater (30 ml.) and ethyl acetate (60 ml.) were added to the residue
4. 4
   その他The aqueous layer was separated
5. 5
   workup.ADDITIONethyl acetate (90 ml.) was added to the aqueous solution
6. 6
   温度cooling
7. 7
   その他the ethyl acetate layer was separated
8. 8
   抽出The remaining aqueous layer was extracted with ethyl acetate (30 ml.)
9. 9
   抽出the extract
10. 10
    洗浄washed with an aqueous solution of sodium chloride
11. 11
    その他dried
12. 12
    濃縮concentrated under reduced pressure
13. 13
    洗浄The residue was washed with diisopropyl ether

実験手順

10% Palladium carbon (0.6 g.) was added to a solution of p-nitrobenzyl 7-{2-(2-formamido-4-thiazolyl)-2-methoxyiminoacetamido}-3-chloro-3-cephem-4-carboxylate (anti isomer, 1.16 g.) in methanol (20 ml.) and tetrahydrofuran (40 ml.), and the mixture was subjected to catalytic reduction at room temperature under atmospheric pressure for 5 hours. After removing the catalyst from the reaction mixture, the filtrate was concentrated under reduced pressure. Water (30 ml.) and ethyl acetate (60 ml.) were added to the residue, and the mixture was adjusted to pH 7.5 with an aqueous solution of sodium bicarbonate and shaked sufficiently. The aqueous layer was separated and ethyl acetate (90 ml.) was added to the aqueous solution. The aqueous layer was adjusted to pH 2.5 with 10% hydrochloric acid with stirring under ice-cooling, and the ethyl acetate layer was separated. The remaining aqueous layer was extracted with ethyl acetate (30 ml.), and the extract and the ethyl acetate layer were combined together, washed with an aqueous solution of sodium chloride, dried and then concentrated under reduced pressure. The residue was washed with diisopropyl ether to give 7-{2-(2-formamido-4-thiazolyl)-2-methoxyiminoacetamido}-3-chloro-3-cephem-4-carboxylic acid (anti isomer, 0.47 g.). The compound was colored at 210° C. and decomposed at above than 250° C.

出典