Pyridine → N-((4aS,5S,7aS)-7a-(2-fluorophenyl)-5-(trifluoromethyl)-4a,5,7,7a-tetrahydro-4H-furo[3,4-d][1,3]thiazin-2-yl)benzamide

温度

-20 °C

A solution of N-((3S,4R,5S)-3-(2-fluorophenyl)-4-(hydroxymethyl)-5-(trifluoromethyl)-tetrahydrofuran-3-ylcarbamothioyl)benzamide (258.3 g, 583.8 mmol) in CH2Cl2 (1.55 L) was cooled to −19.4° C. Pyridine (118 mL, 1.46 mol) was added while maintaining temperature at −20° C., and then the reaction mixture was cooled to −24° C. In another nitrogen purged vessel, CH2Cl2 (258 mL) was added followed by trifluoromethanesulfonic anhydride (108.0 mL, 642.2 mmol). The resulting solution was added to the reaction mixture over 30 min, while maintaining temperature <−19.7° C. Upon completed addition, the reaction mixture was stirred for 30 min at −20° C. to −15° C., and then warmed to −11° C. over 20 min. Saturated aq. NH4Cl (646 mL) and water (390 mL) was added. The mixture was warmed to ambient temperature and the aq. layer was removed. The organics were washed with premixed saturated aq. NH4Cl (646 mL) and water (390 mL). The aq. layers were combined, and extracted once with CH2Cl2 (520 mL). The organics were combined, and concentrated under vacuum to afford a light orange foam (250 g, 100%). The residue was used in the next stage without purification. 1H NMR (500 MHz, CDCl3) δ ppm 8.03 (d, J=6.7 Hz, 2H), 7.52 (t, J=7.0 Hz, 1H), 7.48-7.31 (m, 4H), 7.20 (t, J=7.4 Hz, 1H), 7.12 (dd, J=12.0, 8.4 Hz, 1H), 4.82-4.73 (m, 1H), 4.60 (d, J=8.9 Hz, 1H), 4.03 (d, J=8.3 Hz, 1H), 3.57 (d, J=2.7 Hz, 1H), 3.20 (d, J=13.6 Hz, 1H), 2.81 (dd, J=13.8, 2.5 Hz, 1H); 13C NMR (125 MHz, CDCl3) δ ppm 171.50, 159.57 (d, JCF=247.2 Hz), 134.62, 132.49, 130.65 (d, JCF J=8.8 Hz), 129.77, 128.51, 128.45, 125.14 (q, JCF=281.8 Hz), 124.97 (d, JCF=3.0 Hz), 124.66 (d, JCF=10.3 Hz), 117.05 (d, JCF=23.5 Hz), 66.81 (d, JCF=5.2 Hz), 38.90, 23.20.

1. temperaturethe reaction mixture was cooled to −24° C
2. additionThe resulting solution was added to the reaction mixture over 30 min
3. temperaturewhile maintaining temperature <−19.7° C
4. additionaddition
5. temperaturewarmed to −11° C. over 20 min
6. temperatureThe mixture was warmed to ambient temperature
7. customthe aq. layer was removed
8. washThe organics were washed with premixed saturated aq. NH4Cl (646 mL) and water (390 mL)
9. extractionextracted once with CH2Cl2 (520 mL)
10. concentrationconcentrated under vacuum

ORDレコード

ord-6be822fbcf0e4e5fb7630a441ab93501

出典データセット

uspto-grants-2015_01

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08940734B2