HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromopropylamine hydrobromide → HCID 29799054, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromopropylamine hydrobromide | HCID 78701 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86676372 | HCID 86676372 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 29799054 | HCID 29799054 | 47.4% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 5-(((2,6-dichloropyrimidin-4-yl)oxy)methyl)-2-(3-(trifluoromethyl)phenoxy)benzonitrile (600 mg, 1.363 mmol) and DIPEA (1.5 mL, 8.59 mmol) in N,N-dimethylformamide (3 ml) was added 3-bromopropan-1-amine hydrobromide (900 mg, 4.11 mmol) at 0° C. and the reaction mixture was stirred overnight at 0° C. The solution was purified with reverse phase column chromatography (120 g) using water (contained 0.3% TFA) and MeCN as eluent to afford 5-(((6-(3-bromopropyl)amino)-2-chloropyrimidin-4-yl)oxy)methyl)-2-(3-(trifluoromethyl)phenoxy)benzonitrile (350 mg, 0.646 mmol, 47.4% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09273054B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-dfafcf00ec9b4aab88624aa7da4d43d7 |
| Source note | uspto-grants-2016_03 |