HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxyisovaleric acid → HCID 44200876, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxyisovaleric acid | HCID 69362 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 178422078 | HCID 178422078 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 44200876 | HCID 44200876 | — |
Reaction Steps
To a solution of 3-hydroxy-3-methylbutanoic acid (6 mg, 0.06 mmol) in DMF (1 mL) were added DIPEA (31 μL, 0.18 mmol) and HATU (23 mg, 0.06 mmol). After stirring at rt for 15 min, 17 (20 mg, 0.06 mmol) was added as a solution in DMF (0.5 mL). The reaction was stirred at rt until complete consumption of 17 was determined by LC/MS and then heated at 100° C. for 1 h. Subsequently the reaction was cooled to rt, filtered and purified by preparative LC/MS to give 3-(5-(5-(2-hydroxy-2-methylpropyl)-1,2,4-oxadiazol-3-ylamino)-2-methylphenyl)-1,7-dimethyl-1,6-naphthyridin-2(1H)-one (A56). MS m/z 420.4 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08278452B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-a3bbafea14b04892bbfb1e6258a866f3 |
| Source note | uspto-grants-2012_10 |