N,N-Dimethylaniline → HCID 53857268, compound

1-(1-Carboxy-2-methylpropyl)-3-phenylacetamido-2-azetidinone (1.52 g.) and N,N-dimethylaniline (2.15 g.) were suspended in methylene chloride (12 ml.), and to the suspension was added trimethylsilyl chloride (0.88 g.). The solution was stirred for 30 minutes at ambient temperature and cooled to -50° C. Phosphorus pentachloride (1.1 g.) was added to the solution and the solution was stirred for 2 hrs. (the reaction temperature was elevated to about -30° C. during the stirring.). The solution was cooled to -50° C., and n-butyl alcohol (1.85 g.) was added to the solution, and then the solution was stirred for 2 hrs. (in this time, the reaction temperature was elevated to about -30° C.). The solution was cooled again to -50° C., and a solution preparing by dissolving sodium bicarbonate (1.3 g) in water (15 ml.), was added to the solution (in this time, the reaction temperature was elevated to about -25° C., and the solution indicated about pH 3). The solution was adjusted to pH 4 with sodium bicarbonate, and then the aqueous layer was separated out and washed with ether. The solution was evaporated to dryness under reduced pressure, keeping the temperature of the solution under 25° C. To the residue obtained was added isopropyl alcohol (15 ml.), and the mixture was filtered to obtain an insoluble material and a filtrate. The filtrate was evaporated to dryness under reduced pressure. This operation was repeated twice to give colorless powdery 3-amino-1-(1-carboxy-2-methylpropyl)-2-azetidinone (0.3 g.). These insoluble materials in isopropyl alcohol obtained above were combined and dissolved in a small amount of water, and the solution was adjusted to pH 2.5 with 1 N-hydrochloric acid. The aqueous solution was evaporated to dryness under reduced pressure at 25° C., and the residue obtained was treated with isopropyl alcohol in the similar manner as described above to recover an object compound (0.13 g.). Total yield was 0.43 g. This product was treated in a conventional manner to give its salt of D-camphor-10-sulfonic acid, and the salt was recrystallized from a mixture of acetone and ether to give D-camphor-10-sulfonic acid salt of the object compound. Mp 178° to 183° C.

1. temperaturecooled to -50° C
2. stirringthe solution was stirred for 2 hrs
3. customwas elevated to about -30° C. during the stirring
4. temperatureThe solution was cooled to -50° C.
5. stirringthe solution was stirred for 2 hrs
6. customwas elevated to about -30° C.
7. temperatureThe solution was cooled again to -50° C.
8. customa solution preparing
9. additionwas added to the solution (in this time
10. customwas elevated to about -25° C.
11. customthe aqueous layer was separated out and
12. washwashed with ether
13. customThe solution was evaporated to dryness under reduced pressure
14. customunder 25° C
15. customTo the residue obtained
16. filtrationthe mixture was filtered
17. customto obtain an insoluble material
18. customThe filtrate was evaporated to dryness under reduced pressure

ORD record

ord-a497f35534534aa8a1e94d0ff1789475

Source dataset

uspto-grants-1980_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04207234