HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 2-Acetamido-5-bromopyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | 2-Amino-5-bromopyrimidine | HCID 231310 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Acetamido-5-bromopyrimidine | HCID 22593724 | 70% |
Reaction Steps
To a solution of 5-bromo-2-aminopyrimidine (2.0 g, 11.5 mmole) in CH2Cl2 (75 mL) at RT was added 2,6-lutidine (2.7 mL, 23.0 mmole) followed by acetyl chloride (0.99 g, 12.6 mmole). After stirring for 8 hours, the reaction solution was concentrated under vacuum. The remaining residue was dissolved EtOAc (200 mL), washed with H2O (100 mL) and brine, and dried over Na2SO4. Flash chromatography on silica gel (95:5 CHCl3/MeOH) and drying under high vacuum gave the title compound (1.74 g, 70%) as a yellow solid: MS (ES) m/e 217 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08173646B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-f83244227ccc45378626a321f932eb2c |
| Source note | uspto-grants-2012_05 |