4-Toluenesulfonyl chloride → HCID 178507321, 화합물

To 720 mg. (31 mmoles) of sodium dissolved in 60 ml. of absolute ethanol at room temperature was added 4.59 g. (30.4 mmoles) of 1-(2-amino-4-pyridyl)-1-ethanone oxime, and the resulting mixture allowed to stir for about 5 minutes. To the resulting solution was added 6.10 g. (32 mmoles) of p-toluenesulfonyl chloride and the reaction mixture allowed to stir for 1 hour under a nitrogen atmosphere. The mixture was then added directly to a solution of potassium ethoxide (prepared by dissolving 1.41 g. of potassium in 30 ml. of ethanol) in ethanol and the reaction mixture allowed to stir under a nitrogen atmosphere at room temperature for 0.5 hour. The resulting gelatinous suspension was diluted with 800 ml. of diethyl ether, stirred at room temperature for 0.5 hour and filtered through celite. The filtrate was concentrated, and the residue taken up in 100 ml. of ether which was then extracted with 2 N hydrochloric acid (4×25 ml.). The combined acid extracts were concentrated to a yellow solid, which was dissolved in 60 ml. of water containing 5.83 g. (60 mmoles) of potassium thiocyanate. The resulting solution was heated at steam bath temperatures for 2 hours. On cooling a solid precipitated which was filtered and stirred in 40 ml. of a saturated sodium bicarbonate solution for 0.5 hour. The solids were filtered, washed with water and dried in vacuo to give 3.21 g. (55%) of the product as a yellow solid, m.p. 262°-264° C. The analytical sample was recrystallized from water.

1. additionTo the resulting solution was added 6.10 g
2. stirringto stir for 1 hour under a nitrogen atmosphere
3. stirringto stir under a nitrogen atmosphere at room temperature for 0.5 hour
4. additionThe resulting gelatinous suspension was diluted with 800 ml
5. filtrationfiltered through celite
6. concentrationThe filtrate was concentrated
7. extractionof ether which was then extracted with 2 N hydrochloric acid (4×25 ml.)
8. concentrationThe combined acid extracts were concentrated to a yellow solid, which
9. dissolutionwas dissolved in 60 ml
10. temperatureThe resulting solution was heated at steam bath temperatures for 2 hours
11. temperatureOn cooling a solid
12. customprecipitated which
13. filtrationwas filtered
14. stirringstirred in 40 ml
15. waitof a saturated sodium bicarbonate solution for 0.5 hour
16. filtrationThe solids were filtered
17. washwashed with water
18. customdried in vacuo
19. customto give 3.21 g
20. customThe analytical sample was recrystallized from water

ORD 기록

ord-edec831f00c04300a8061063a89f4e02

출처 데이터셋

uspto-grants-1981_11

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US04302464