HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 57531447, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 57531599 | HCID 57531599 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 57531447 | HCID 57531447 | — |
Reaction Steps
To a vial containing (1S)-N-{[4-(aminomethyl)-2-(2,6-diethylphenyl)-6-methylpyrimidin-5-yl]methyl}-N-methyl-1,2,3,4-tetrahydronaphthalen-1-amine (9 mg, 0.021 mmol) in CHCl3 (2.0 mL) is added acetic anhydride (0.05 mL, 25.0 eq., 0.53 mmol) and allowed to stir at room temperature for 2 h. All solvent is then removed and excess acetic anhydride is removed azeotropically with toluene (3×2 mL). The sample is re-dissolved in CHCl3 and eluted through a plug of SiO2, washing with CHCl3. Concentration affords the title compound as a colorless gum. [mass expected (470.65); mass found (470.34)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07482350B2 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-db07e66829b74e9e912f73dab58a2b21 |
| Source note | uspto-grants-2009_01 |