Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 18628958 | HCID 18628958 | — |
| Reactant | HCID 90072119 | HCID 90072119 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 90088631 | HCID 90088631 | 41.7% |
Reaction Steps
In a 1 L round-bottomed flask, a solution of 2-(1H-benzo[d][1,2,3]triazol-1-yl)-2-((phenoxycarbonyl)amino)acetic acid (19.37 g, 62.0 mmol) in THF (135 mL) was cooled in ice/water bath and treated with oxalyl chloride (5.43 mL, 62.0 mmol) and 4 drops DMF (bubbling). The reaction mixture was stirred for 4 hours (until HPLC analysis showed complete conversion to acid chloride). Then a solution of (2-amino-3-methylphenyl)(3-fluorophenyl)methanone (7.11 g, 31.0 mmol) in THF (35 mL) was added with 5 mL THF rinse and the resulting solution was removed from ice/water bath and stirred at room temperature for 1.5 hours. The mixture was then treated with a solution of ammonia, 7M in MeOH (19.94 mL, 140 mmol) (slight exotherm, immediately a white precipitate formed and mixture was cooled in ice/water bath). After 15 mins another portion of ammonia, 7M in MeOH (19.94 mL, 140 mmol) was added and the resulting mixture was removed from ice/water bath and sealed under N2 and stirred overnight at room temperature. The reaction mixture was concentrated to ˜½ volume and the resulting mixture was diluted with AcOH (63 mL) and stir at room temperature for 4 hours (until HPLC analysis showed complete conversion). The reaction mixture was concentrated and the residue dilute with 500 mL water and to give an orange sticky precipitate. Hexane and Et2O was added and stir at room temperature for 1 hour to form an orange solid. Et2O was removed under a stream of nitrogen and the aqueous layer was decanted. The orange sticky residue was triturate with 40 mL iPrOH and stir at room temperature to give a white precipitate. The solid was filtered and washed with iPrOH, dried on filter frit under a stream of nitrogen to give benzyl (5-(3-fluorophenyl)-9-methyl-2-oxo-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)carbamate (5.4 g, 41.7% yield). MS(ES):m/z=418.3 [M+H+]; HPLC: RT=3.075 min Purity=99%. (H2O/MeOH with TFA, CHROMOLITH® ODS S5 4.6×50 mm, gradient=4 min, wavelength=220 nm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09133139B2 |
|---|
| Source dataset | uspto-grants-2015_09 |
|---|
| ORD ID | ord-c24886764d724a69b0fb6c2580098a60 |
|---|
| Source note | uspto-grants-2015_09 |
|---|