HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 56650038, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (-)-Mandelic acid | HCID 11914 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | HCID 66747984 | HCID 66747984 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 56650038 | HCID 56650038 | — |
Reaction Steps
To a mixture of 4-isobutoxy-6-(piperazin-1-yl)pyrimidine dihydrochloride (30 mg, 0.097 mmol), (R)-2-hydroxy-2-phenylacetic acid (15 mg, 0.097 mmol), and triethylamine (0.07 mL, 0.49 mmol) in DMF was added HBTU (48 mg, 0.13 mmol), and the mixture was stirred at rt for 1 h. Then the mixture was poured onto water (3 mL), and the aqueous layer was extracted with dichloromethane (three times). The combined organic layers were dried over sodium sulfate and concentrated in vacuo. The residue was purified by preparative LC-MS to give 7.2 mg (15% yields) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08999974B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-5033453dadd645b88de9334a03d231c3 |
| Source note | uspto-grants-2015_04 |