Triethylamine → HCID 59596988, compound

4-(4-Nitrophenoxy)pyridin-2-ylamine (100 mg) was dissolved in tetrahydrofuran (5 ml) under a nitrogen atmosphere, triethylamine (0.181 ml) and phenyl chloroformate (0.163 ml) were added while stirring and cooling in an ice water bath. The reaction mixture was allowed to warm up to room temperature and stirred for 30 min. The reaction mixture was partitioned between ethyl acetate (50 ml) and a saturated aqueous solution of sodium hydrogencarbonate (30 ml). The separated organic layer was washed with water (30 ml) and brine (30 ml) in this order, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure. To the residue was added N,N-dimethylformamide (5 ml), and azetidine monohydrochloride (203 mg) and triethylamine (0.483 ml) were added, followed by stirring overnight. The reaction mixture was concentrated under reduced pressure, the resultant residue was partitioned after addition of ethyl acetate (50 ml) and a saturated aqueous solution of ammonium chloride (30 ml). The separated organic layer was washed with a saturated aqueous solution of ammonium chloride (30 ml), water (30 ml) and brine (30 ml), and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified by silica gel column chromatography (eluent; heptane:ethyl acetate=1:3, then ethyl acetate). Fractions containing the target compound were concentrated under reduced pressure to provide the roughly-purified titled compound as a pale yellow solid (118.7 mg).

1. temperaturecooling in an ice water bath
2. stirringstirred for 30 min
3. customThe reaction mixture was partitioned between ethyl acetate (50 ml)
4. washThe separated organic layer was washed with water (30 ml) and brine (30 ml) in this order
5. dry with materialdried over anhydrous sodium sulfate
6. customThe solvent was removed under reduced pressure
7. additionTo the residue was added N,N-dimethylformamide (5 ml), and azetidine monohydrochloride (203 mg) and triethylamine (0.483 ml)
8. additionwere added
9. stirringby stirring overnight
10. concentrationThe reaction mixture was concentrated under reduced pressure
11. customthe resultant residue was partitioned
12. additionafter addition of ethyl acetate (50 ml)
13. washThe separated organic layer was washed with a saturated aqueous solution of ammonium chloride (30 ml), water (30 ml) and brine (30 ml)
14. dry with materialdried over anhydrous sodium sulfate
15. customThe solvent was removed under reduced pressure
16. customthe residue was purified by silica gel column chromatography (eluent
17. additionFractions containing the target compound
18. concentrationwere concentrated under reduced pressure
19. customto provide the
20. customroughly-purified titled compound as a pale yellow solid (118.7 mg)

ORD record

ord-964c8a8343fb4f6d8291d35c01a34b81

Source dataset

uspto-grants-2010_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07855290B2