HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycine → HCID 52947078, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glycine | HCID 750 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Cyano-borohydride | HCID 498716 | — |
| Reactant | HCID 86619632 | HCID 86619632 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 52947078 | HCID 52947078 | — |
| Product | HCID 86619635 | HCID 86619635 | — |
Reaction Steps
To a stirred solution of 4-(3-oxo-propyl)-6-(3-trifluoromethylphenyl)-pyrimidine-2-carbonitrile (50 mg) in methanol (1 mL) was added glycine (25 mg), followed by water (100 μL) and acetic acid (12 μL). The mixture was stirred at room temperature for five minutes then solid supported cyanoborohydride (77 mg, 2.57 mmol/g) was added and stirring continued overnight. The reaction mixture was filtered and the filtrate concentrated under reduced pressure to yield crude product. Purification by preparative-HPLC afforded the TFA salt of 4-[3-(carboxymethyl-amino)-propyl]-6-(3-trifluoromethylphenyl)-pyrimidine-2-carbonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07589095B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-eefa024743b148929e036cd54d6b8433 |
| Source note | uspto-grants-2009_09 |