Tris(1,1-dimethylethyl)phosphine → 1,1-Dimethylethyl 4-(6-amino-3,4-dihydro-1(2H)-quinolinyl)-1-piperidinecarboxylate

A suspension of Pd2(dba)3 (29 mg, 0.032 mmol) in 2 mL anhydrous THF was treated with PtBu3 (400 μL of a 10% wt in hexanes solution, 0.13 mmol) and stirred at room temperature for 5 minutes. To this mixture was added tert-butyl 4-(6-bromo-3,4-dihydroquinolin-1(2H)-yl)piperidine-1-carboxylate (250 mg, 0.63 mmol) followed by lithium hexamethyldisilizane (1.3 mL of a 1 M solution in THF, 1.3 mmol). The resulting dark brown suspension was heated at 95° C. for 3 hours. The mixture was cooled to room temperature and treated with 5 ml of a 1M tetrabutylammonium fluoride solution in THF then stirred at room temperature for 30 minutes. The mixture was partitioned between ethyl acetate (100 mL) and H2O (20 mL). After extraction, the organic layer was separated, dried over Na2SO4, filtered and concentrated to give a dark brown residue. This residue was subjected to flash chromatography on silica gel using 2.5% 2M NH3 in methanol/CH2Cl2 to give a viscous dark brown residue (160 mg, 76.6%). 1H-NMR (CDCl3) δ 6.56 (d, J=8.4 Hz, 1H), 6.48 (dd, J=2.7, 8.7 Hz, 1H), 6.43-6.42 (m, 1H), 4.25-4.21 (m, 2H), 3.69-3.59 (m, 1H), 3.24 (br s, 2H), 3.07 (t, J=5.4 Hz, 2H), 2.78-2.72 (m, 2H), 2.66 (t, J=6.6 Hz, 2H), 1.93-1.83 (m, 2H), 1.76-1.55 (m, 4H), 1.47 (s, 9H). MS (ESI): 332.2 (M+1, 100%).

1. temperatureThe resulting dark brown suspension was heated at 95° C. for 3 hours
2. temperatureThe mixture was cooled to room temperature
3. stirringthen stirred at room temperature for 30 minutes
4. customThe mixture was partitioned between ethyl acetate (100 mL) and H2O (20 mL)
5. extractionAfter extraction
6. customthe organic layer was separated
7. dry with materialdried over Na2SO4
8. filtrationfiltered
9. concentrationconcentrated
10. customto give a dark brown residue

ORDレコード

ord-85ccace87ec94ae29e72660017315408

出典データセット

uspto-grants-2012_05

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08173813B2