HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 4-bromo-2-fluoro-N-(pyrimidin-2-ylmethyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Bromo-2-fluorobenzoic acid | HCID 302681 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | 2-Pyrimidinemethanamine | HCID 4658047 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-bromo-2-fluoro-N-(pyrimidin-2-ylmethyl)benzamide | HCID 118045701 | 29.3% |
Reaction Steps
To a flask was charged with 4-bromo-2-fluorobenzoic acid (180 mg, 0.821 mmol), pyrimidin-2-ylmethanamine (89.6 mg, 0.821 mmol), DIEA (0.358 mL, 2.05 mmol) in DMF (3 mL), and to the resulting solution was added PyBOP (513 mg, 0.915 mmol) and the resulting mixture was stirred at room temperature overnight, then was concentrated under reduced pressure and the residue was diluted with EtOAc (20 mL), washed with water (3×10 mL), brine (10 mL) and dried (Na2SO4), concentrated and the residue was purified by flash chromatography on silica gel eluted with gradient EtOAc/heptane (0-100%) and 4-bromo-2-fluoro-N-(pyrimidin-2-ylmethyl)benzamide (74.5 mg, 29.3%) was obtained as light color solid. LCMS (m/z): 310.0/312.0 (MH+), 0.64 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242996B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-bbbb1bd250ff4f17b79b7994733f1a00 |
| Source note | uspto-grants-2016_01 |