Piperidine → Ethyl (9aS)-2-[2-(4-fluorophenyl)ethyl]-4-[3-fluoro-4-({[(1S)-1-(4-pyridinyl)ethyl]amino}carbonyl)phenyl]-5-oxo-7,8,9,9a-tetrahydro-5H-pyrido[2,3-a]pyrrolizine-3-carboxylate

tert-Butyl (2S)-2-(3-ethoxy-3-oxopropanoyl)-1-pyrrolidinecarboxylate (0.096 g, 0.22 mmol, 1 equiv), ethyl (2Z)-3-amino-5-(4-fluorophenyl)-2-pentenoate (0.052 g, 0.22 mmol, 1 equiv), 4-carboxy-3-fluorobenzaldehyde (0.037 g, 0.22 mmol, 1 equiv), and piperidine (0.011 mL, 0.11 mmol, 0.5 equiv) were combined in toluene (0.5 mL). After 2 h at 90° C., the reaction was cooled to ambient temp. CAN (0.24 g, 0.44 mmol, 2 equiv) and H2O (0.5 mL) were added. After 0.5 h the layers were separated. The aqueous portion was extracted with EtOAc (2×1 mL) and the combined organic portions were concentrated to a brown oil. The crude oil was then treated with 4 N HCl in dioxane (1.0 mL). After 1 h, the mixture was concentrated to a brown oil. A CH2Cl2 solution (1.0 mL) of this crude oil was treated with Et3N (0.15 mL, 1.10 mmol, 5 equiv). After 8 h, the mixture was concentrated to a brown foam. A solution of the crude foam (0.028 g, 0.06 mmol, 1 equiv) in CH2Cl2 (0.5 mL) was treated with (−)-α-4-(pyridyl)ethylamine (0.015 g, 0.12 mmol, 2 equiv), EDCI (0.013 g, 0.07 mmol, 1.2 equiv), and HOBt (0.009 g, 0.07 mmol, 1.2 equiv). After 12 h at ambient temperature, the reaction was diluted with CH2Cl2 (1.0 mL) and treated with saturated aqueous NaHCO3 (1 mL). The organic portion was the washed with 1N HCl (1 mL) followed by brine (1 mL). Concentration gave a brown oil that was chromatographed radially (SiO2, 1 mm plate, EtOAc) to provide the title compound as a pale yellow foam (0.020 g, 59%): 1H NMR (CDCl3, 400 MHz) δ 8.60 (d, J=5.1 Hz, 2H), 8.08 (t, J=8.2 Hz, 1H), 7.40 (d, J=5.2 Hz, 2H), 7.25–7.21 (m, 2H), 7.17–7.13 (m, 2H), 7.06–7.03 (m, 1H), 6.95 (t, J=8.6 Hz, 2H), 5.33–5.30 (m, 1H), 4.72 (dd, J=10.3, 6.3 Hz, 1H), 4.10–4.02 (m, 2H), 3.74–3.67 (m, 1H), 3.41–3.35 (m, 1H), 3.20–3.02 (m, 4H), 2.50.2.45 (m, 1H), 2.37–2.29 (m, 2H), 1.60 (d, J=7.2 Hz, 3H), 1.43–1.33 (m, 1H), 1.00 (t, J=7.1 Hz, 3H); low resolution MS (ES+) m/e 611 (MH+); RP-HPLC (Dynamax C-18 25 cm×4.1 mm; 50–100% CH3CN in H2O with 0.1% TFA buffer; 30 minutes; 1 mL/min) tr=6.37 min, 95% purity.

1. customAfter 0.5 h the layers were separated
2. extractionThe aqueous portion was extracted with EtOAc (2×1 mL)
3. concentrationthe combined organic portions were concentrated to a brown oil
4. additionThe crude oil was then treated with 4 N HCl in dioxane (1.0 mL)
5. waitAfter 1 h
6. concentrationthe mixture was concentrated to a brown oil
7. waitAfter 8 h
8. concentrationthe mixture was concentrated to a brown foam
9. waitAfter 12 h at ambient temperature
10. washwashed with 1N HCl (1 mL)
11. concentrationConcentration
12. customgave a brown oil that
13. customwas chromatographed radially (SiO2, 1 mm plate, EtOAc)

ORD record

ord-a843221fb9f44b1ead1e2c2945c5393c

Source dataset

uspto-grants-2007_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07189851B2