HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → Methyl 2-(((benzyloxy)carbonyl)(7-(trifluoromethyl)isoquinolin-1-yl)amino)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | Benzyl (7-(trifluoromethyl)isoquinolin-1-yl)carbamate | HCID 58562812 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-(((benzyloxy)carbonyl)(7-(trifluoromethyl)isoquinolin-1-yl)amino)acetate | HCID 58562656 | — |
Reaction Steps
A solution of benzyl (7-(trifluoromethyl)isoquinolin-1-yl)carbamate (212 mg, 0.61 mmol), from above step F in DMF (5 mL) was cooled in an ice bath and treated with NaH (27 mg, 0.67 mmol), and the mixture was stirred for 30 min and was treated with methyl bromoacetate (64 μL, 0.67 mmol). This solution was stirred and allowed to warm to room temperature over 18 h. The reaction was quenched with saturated NH4Cl and DMF was removed under vacuum. The residue was taken in EtOAc and washed with water, sat NaCl and dried over Na2SO4. EtOAc was removed under vacuum and the residue was purified by silica column chromatography to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09062048B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-b90c7c23a67f4b798e14ebbf7af08354 |
| Source note | uspto-grants-2015_06 |