Hydrochloric Acid → 3-[1-(2-Aminoethyl)-1,2,3,6-tetrahydropyridin-4-yl]-7-[(R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy]-furo[3,2-c]pyridin-6-ylamine

A mixture of 7-[(R)-1-(2,6-Dichloro-3-fluorophenyl)ethoxy]-3-(1,2,3,6-tetrahydropyridin-4-yl)-furo[3,2-c]pyridin-6-ylamine (35.0 mg, 0.0829 mmol), tert-butyl N-(2-oxoethyl)carbamate (26.4 mg, 0.166 mmol), sodium triacetoxyborohydride (19.3 mg, 0.0912 mmol) and DCM (3 mL, 50 mmol) was stirred at rt for 30 min. The solution was transferred to a separatory funnel and extracted with DCM and sat. NaHCO3. The organic layer was concentrated in vacuo, redissolved in 1,4-dioxane and transferred to a sealed tube. 4 M of HCl in 1,4-Dioxane (0.5 mL, 2 mmol) was added, and the mixture was heated to 50° C. for 2 h. The solution was concentrated in vacuo, redissolved in DCM and transferred to a separatory funnel. The organic layer was washed with sat. NaHCO3, concentrated in vacuo, and loaded onto a prep TLC plate, eluting with 7% (7N NH3 in MeOH)/DCM. The band containing the pure product was filtered off using 1:1 MeOH/DCM. To the filtrate was added 2.0 M of HCl in Et2O (0.207 mL, 0.414 mmol) to form the HCl salt, and the mixture was stirred for 30 min at rt. The material was concentrated in vacuo to afford the title compound as bis-HCl salt. 1H NMR (CD3OD, 400 MHz): δ=1.88 (d, J=6.8 Hz, 3H), 2.56 (d, J=1.5 Hz, 2H), 2.79 (ddd, J=19.3, 5.8, 5.7 Hz, 4H), 3.12 (t, J=5.9 Hz, 2H), 3.28 (d, J=2.5 Hz, 2H), 6.27 (br, s, 1H), 6.50 (q, J=6.8 Hz, 1H), 7.22 (t, J=8.6 Hz, 1H), 7.40 (dd, J=9.0, 4.9 Hz, 1H), 7.63 (s, 1H), 8.17 (s, 1H). MS (ES+): m/z 465.04 [MH+]. HPLC: tR=2.43 min (ZQ3, polar—5 min).

1. customThe solution was transferred to a separatory funnel
2. extractionextracted with DCM and sat. NaHCO3
3. concentrationThe organic layer was concentrated in vacuo
4. dissolutionredissolved in 1,4-dioxane
5. customtransferred to a sealed tube
6. temperaturethe mixture was heated to 50° C. for 2 h
7. concentrationThe solution was concentrated in vacuo
8. dissolutionredissolved in DCM
9. customtransferred to a separatory funnel
10. washThe organic layer was washed with sat. NaHCO3
11. concentrationconcentrated in vacuo
12. washeluting with 7% (7N NH3 in MeOH)/DCM
13. additionThe band containing the pure product
14. filtrationwas filtered off

ORD 기록

ord-4ccc76bda2ce40a9bc9e94b754552319

출처 데이터셋

uspto-grants-2011_09

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US08022206B2