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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570913Generated: October 28, 2026

HCID 89601756, compound → HCID 89602037, compound

https://huagongshe.com/reaction/570913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 89601756HCID 89601756—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
ProductHCID 89602037HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024019B2
Source datasetuspto-grants-2015_05
ORD IDord-55ec291e216b48debb08faea94e36022
Source noteuspto-grants-2015_05