HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 89601756, compound → HCID 89602037, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 89601756 | HCID 89601756 | — |
| Reactant | HCID 178418689 | HCID 178418689 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 89602037 | HCID 89602037 | — |
Reaction Steps
To a solution of tert-butyl 4-[acetyl(tert-butoxycarbonyl)amino]-6-formyl-3-oxo-5H-1,2,4-triazine-2-carboxylate (1.15 g, 3.00 mmol) [prepared according to Example 1, Step F] in THF (11.0 mL) at 0° C. was slowly added MeMgBr (3M solution in Et2O, 1.50 mL, 4.50 mmol) via syringe. The reaction mixture was allowed to warm to room temperature and stirred for another 20 h. The reaction mixture was quenched with sat NH4Cl solution and the aqueous layer extracted EtOAc. After washing of the combined organic layers with brine and drying (Na2SO4), the solvent was removed in vacuo to give the desired product as a viscous oil. LCMS (Method I) RT 1.19 min. [M+Na]+ 323.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09024019B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-55ec291e216b48debb08faea94e36022 |
| Source note | uspto-grants-2015_05 |