Iodine → 3-(3-(Cyclopropylmethoxy)phenyl)pentan-3-amine

To a solution of magnesium (280 mg) in THF (2.5 mL), iodine (10 mg) was added at room temperature. Then, a small amount of a solution of 1-bromo-3-(cyclopropylmethoxy)benzene (2.27 g) obtained according to a method described in the document (Izvestiya akademi Nauk SSSR, Seriya Khimicheskaya, 12, 2752-2755 (1989)) in THF (3.5 mL) was added thereto, and the mixture was stirred at room temperature for 10 minutes until the iodine color disappeared. The remaining amount of the solution of 1-bromo-3-(cyclopropylmethoxy)benzene in THF was added thereto, and the mixture was stirred at room temperature for 1 hour until the magnesium disappeared. To the reaction mixture, a solution of 3-pentanone (1.02 g) in THF (3.0 mL) was added, and the mixture was stirred at room temperature for 2 hours. To the reaction mixture, an aqueous saturated ammonium chloride solution (10 ml) was added at 0° C., and the aqueous layer was extracted with ethyl acetate (20 mL×2). The organic layer was washed with brine (20 mL), dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (30% ethyl acetate/hexane). The obtained compound was dissolved in chloroform (20 mL). To the solution, sodium azide (1.7 g) was added. To the reaction mixture, trifluoroacetic acid (3.2 mL) was added dropwise at 0° C., and the mixture was then stirred at room temperature for 1 hour. To the reaction mixture, water (20 mL) was added, and the resultant mixture was then extracted with chloroform (20 mL). The organic layer was washed with an aqueous saturated sodium bicarbonate solution (20 mL), dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (10% ethyl acetate/hexane). The obtained compound was dissolved in methanol (10 mL). To the solution, 10% palladium-carbon (260 mg) was added, and the reaction mixture was stirred at room temperature for 2 hours under a hydrogen atmosphere. The precipitate was removed by filtration through a pad of Celite and washed with methanol (100 mL). Then, the combined filtrate was concentrated under reduced pressure to obtain the title compound (1.70 g) as a crude product.

1. additionwas added
2. extractionthe aqueous layer was extracted with ethyl acetate (20 mL×2)
3. washThe organic layer was washed with brine (20 mL)
4. dry with materialdried over anhydrous sodium sulfate
5. concentrationconcentrated under reduced pressure
6. customThe residue was purified by silica gel column chromatography (30% ethyl acetate/hexane)
7. dissolutionThe obtained compound was dissolved in chloroform (20 mL)
8. additionTo the solution, sodium azide (1.7 g) was added
9. additionTo the reaction mixture, trifluoroacetic acid (3.2 mL) was added dropwise at 0° C.
10. stirringthe mixture was then stirred at room temperature for 1 hour
11. additionTo the reaction mixture, water (20 mL) was added
12. extractionthe resultant mixture was then extracted with chloroform (20 mL)
13. washThe organic layer was washed with an aqueous saturated sodium bicarbonate solution (20 mL)
14. dry with materialdried over anhydrous sodium sulfate
15. concentrationconcentrated under reduced pressure
16. customThe residue was purified by silica gel column chromatography (10% ethyl acetate/hexane)
17. dissolutionThe obtained compound was dissolved in methanol (10 mL)
18. additionTo the solution, 10% palladium-carbon (260 mg) was added
19. stirringthe reaction mixture was stirred at room temperature for 2 hours under a hydrogen atmosphere
20. customThe precipitate was removed by filtration through a pad of Celite
21. washwashed with methanol (100 mL)
22. concentrationThen, the combined filtrate was concentrated under reduced pressure

ORDレコード

ord-811206affdb240aaaf3ad27aa42223e4

出典データセット

uspto-grants-2013_09

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08530490B2