Water → (E)-(6R,7R)-7-[(R)-2-bromo-propionylamino]-3-[3-(carbamoylmethyl-dimethyl-ammonio)-propenyl]-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylate

To a suspension of 1.4 g (E)-(6R,7R)-7-amino-3-[3-(carbamoylmethyl-dimethyl-ammonio)-propenyl]-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylate monohydroiodide in 24 ml of dichloromethane/acetonitrile (1:1) was added 4 ml of N,O-Bis(trimethylsilanyl)trifluoroacetamide and the mixture was stirred at 20° for 0.5 h. After cooling of the reaction mixture to 0°, 2.05 g of (R)-2-bromo-propionyl chloride was added and stirring was continued for 5 min. The solution was dropped onto 0.5 l of diethyl ether containing 0.2 ml of water. The mixture was stirred for 0.5 h and subsequently, the precipitate was isolated by filtration, washed with 50 ml of diethyl ether, and dried. The brown solid was suspended in 5 ml of water. After adjusting the pH to 2.5 by the addition of 2N NaOH, 0.3 l of 2-propanol were added and the mixture was stirred at 20° for 0.5 h. The precipitate was filtered off, washed with 50 ml of diethyl ether and dried, to give 1.3 g of (E)-(6R,7R)-7-[(R)-2-bromo-propionylamino]-3-[3-(carbamoylmethyl-dimethyl-ammonio)-propenyl]-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylate as a light-brown powder.

1. temperatureAfter cooling of the reaction mixture to 0°
2. stirringstirring
3. waitwas continued for 5 min
4. stirringThe mixture was stirred for 0.5 h
5. customsubsequently, the precipitate was isolated by filtration
6. washwashed with 50 ml of diethyl ether
7. customdried
8. additionby the addition of 2N NaOH, 0.3 l of 2-propanol
9. additionwere added
10. stirringthe mixture was stirred at 20° for 0.5 h
11. filtrationThe precipitate was filtered off
12. washwashed with 50 ml of diethyl ether
13. customdried

ORDレコード

ord-7d04d96c74524ca4b5515a87af0ffb44

出典データセット

uspto-grants-2003_06

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US06583133B1