HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → {[4-Chloro-2-fluoro-3-(1-naphthalenyloxy)phenyl]methyl}amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1-{[3-(Bromomethyl)-6-chloro-2-fluorophenyl]oxy}naphthalene | HCID 68485558 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | {[4-Chloro-2-fluoro-3-(1-naphthalenyloxy)phenyl]methyl}amine | HCID 68486009 | 87% |
Reaction Steps
To a solution of 1-{[3-(bromomethyl)-6-chloro-2-fluorophenyl]oxy}naphthalene (0.96 g, 2.63 mmol) in dichloromethane (10 mL) was added 7N ammonia in methanol (20 mL, 140 mmol). The mixture was stirred at room temperature overnight. The solvent was evaporated and the residue was triturated with dichloromethane to give the desired product (0.769 g, 87%) as an off-white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.29-8.37 (m, 1H), 7.94-8.03 (m, 1H), 7.60-7.71 (m, 4H), 7.56 (t, 1H), 7.36 (t, 1H), 6.56 (d, 1H), 4.13 (s, 2H). ES MS: m/z 302 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08304419B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-78ebd4ad1f844df9b23675073551c2a0 |
| Source note | uspto-grants-2012_11 |