Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | HCID 89771121 | HCID 89771121 | — |
| Reactant | HCID 89771122 | HCID 89771122 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 89771165 | HCID 89771165 | 49.4% |
Reaction Steps
To a solution of triphosgene (72 mg, 0.242 mmol) in EtOAc (5 mL) at 0° C. was added solution of (1S,8aS)-1-o-tolylhexahydropyrrolo[1,2-a]pyrazin-6(7H)-one (112 mg, 0.484 mmol), DMAP (6.2 mg, 0.05 mmol) and TEA (151 mg, 1.5 mmol) in EtOAc (15 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-1-(3-isopropyl-5-(trifluoromethyl)phenyl)-N-methylethanamine (142 mg, 0.58 mmol) in EtOAc (10 mL) and TEA (151 mg, 1.5 mmol). The reaction was then stirred at 50° C. for 48 h and quenched with water. The resulting mixture was extracted with EtOAc. The combined organic layer was washed with 1 N aqueous HCl solution, dried over anhydrous Na2SO4 and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH=20/1 to 10/1) to give the title compound (60 mg, yield: 25%) as yellow solid. 1H-NMR (400 MHz, CDCl3) δ ppm 7.37 (s, 1H), 7.27 (d, J=6 Hz, 2H), 7.15 (m, 5H), 5.48 (m, 1H), 4.08 (m, 2H), 3.71 (m, 1H), 2.87 (m, 4H), 2.67 (s, 3H), 2.56 (s, 3H), 2.37 (m, 2H), 1.82 (m, 1H), 1.64 (m, 1H), 1.35 (d, 3H), 1.22 (m, 3H); m/z (ES+): 502 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09181259B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-067ed7e02c4444378897c5f731893b60 |
|---|
| Source note | uspto-grants-2015_11 |
|---|