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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110216Generated: November 1, 2026

tert-butyl 1-(methoxy(methyl)carbamoyl)-3-phenyl-5,6-dihydroimidazo[1,5-a]pyrazine-7(8H)-carboxylate → tert-butyl 1-(3,3-dimethylbutanoyl)-3-phenyl-5,6-dihydro-imidazo[1,5-a]pyrazine-7(8H)-carboxylate

https://huagongshe.com/reaction/2110216

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 1-(methoxy(methyl)carbamoyl)-3-phenyl-5,6-dihydroimidazo[1,5-a]pyrazine-7(8H)-carboxylateHCID 57635358—
ReactantHCID 178418809HCID 178418809—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl 1-(3,3-dimethylbutanoyl)-3-phenyl-5,6-dihydro-imidazo[1,5-a]pyrazine-7(8H)-carboxylateHCID 5763557377%

Reaction Conditions

Temperature0 °C

Reaction Steps

Compound 26A (0.10 g, 0.26 mmol) was dissolved in THF and cooled to 0° C. and neopentylmagnesium chloride (1M in diethyl ether, 0.35 mL) was added and the mixture was stirred for 2 hours. The mixture was quenched with NH4Cl saturated solution and extracted with EtOAc. The residue was purified by preparative flash chromatography on silica, eluting with 20-80% gradient of ethyl acetate in hexanes to provide intermediate 26B (0.08 g, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517874B2
Source datasetuspto-grants-2009_04
ORD IDord-0b05a32462294a789bb55528a7b8d55d
Source noteuspto-grants-2009_04