HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 57531383, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 57531498 | HCID 57531498 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 57531383 | HCID 57531383 | — |
Reaction Steps
To a vial containing 4-(aminomethyl)-1-[2-(2,6-diethylphenyl)-6-methyl-5-({methyl[(1S)-1,2,3,4-tetrahydronaphthalen-1-yl]amino}methyl)pyrimidin-4-yl]piperidin-4-ol (25 mg, 0.047 mmol) in DMA (1.0 mL) is added K2CO3 (33 mg, 5.0 eq., 0.24 mmol) and acetic anhydride (0.023 mL, 5.0 eq., 0.24 mmol) and allowed to stir at room temperature for 16 h. EtOAc (2.0 mL) and sat NaHCO3 (2.0 mL) are then added and the organic layer is transferred directly onto a SiO2 plate and the product is eluted with 20:1 CHCl3:MeOH affording the title compound as a white foam. [mass expected (569.78); mass found (569.30)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08129395B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-b5f6035ae735489aab29a67c3db5d540 |
| Source note | uspto-grants-2012_03 |