HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 23570707, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | HCID 23570706 | HCID 23570706 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 23570707 | HCID 23570707 | — |
Reaction Steps
To a solution of 0.7 mmol of acetic acid 4-{2-amino-3-oxo-3-[2-(5-phenyl-1H-imidazol-2-yl)-piperidin-1-yl]-propyl}-3,5-dimethyl-phenyl ester and 0.8 mL of formaldehyde, cooled in an ice bath under argon, was added 0.5 mL of acetic acid. The resulting mixture was allowed to slowly return to room temperature and stir overnight. The mixture was then extracted with ethyl acetate. The ethyl acetate was washed with water, dried over magnesium sulfate and concentrated to 0.39 g of an orange-yellow oil which was taken to the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07202381B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-17111ce35b124e329c41915de8339c70 |
| Source note | uspto-grants-2007_04 |