HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → HCID 118483141, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 118483198 | HCID 118483198 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 118483141 | HCID 118483141 | 23% |
Reaction Steps
To a solution of {1-[4-(4-cyano-3-fluoro-phenyl)-1-(3-methoxy-propyl)-6-oxo-1,6-dihydro-pyrimidin-2-yl]-piperidin-4-yl}-carbamic acid tert-butyl ester (200 mg, 0.41 mmol) in DCM was added 1M BBr3 (4 mL) at −78° C. The mixture was stirred at RT for 2 h and quenched at 0° C. with MeOH. The solution was washed with aqueous saturated NaHCO3. The organic layer was dried and concentrated. The residue was purified by preparative HPLC to give 35 mg of the title product as the hydrochloride salt (23%). 1H NMR (400 MHz, CD3OD): 1.65-1.69 (m, 2H), 1.97-2.19 (m, 4H), 3.13-3.22 (m, 2H), 3.48-3.55 (m, 1H), 3.73 (t, J=8.0 Hz, 2H), 4.55 (t, J=8.0 Hz, 2H), 4.94-4.95 (m, 2H), 6.71 (s, 1H), 7.88-8.05 (m, 3H). [M+H] Calc'd for C19H22FN5O2, 371. Found, 371.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09255097B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-51e2f926a5c548458611a32402d4f72f |
| Source note | uspto-grants-2016_02 |