Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244136Generated: October 28, 2026

7-Cyclobutyl-5-(2-phenylquinazolin-7-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine → 3-Cyclobutyl-1-(4-methyl-2-phenyl-quinazolin-7-yl)-imidazo[1,5-a]pyrazin-8-ylamine

https://huagongshe.com/reaction/244136

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Cyclobutyl-5-(2-phenylquinazolin-7-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 53629048—
Reactant1-Bromo-3-cyclobutylimidazo[1,5-a]pyrazin-8-amineHCID 57680934—
Product3-Cyclobutyl-1-(4-methyl-2-phenyl-quinazolin-7-yl)-imidazo[1,5-a]pyrazin-8-ylamineHCID 11524288—

Reaction Steps

Synthesized as 7-cyclobutyl-5-(2-phenylquinazolin-7-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine from of 1-bromo-3-cyclobutylimidazo[1,5-a]pyrazin-8-amine (16 mg, 0.06 mmol). Crude material was purified by preparative TLC (silica gel, 5% MeOH in DCM) followed by a recrystallization (EtOAc) and trituration (hexanes) to afford the title compound as a light yellow solid; MS (ES+): m/z 407.1 (100); HPLC: tR (min) 2.44 (OpenLynx, polar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653268B2
Source datasetuspto-grants-2014_02
ORD IDord-111846e36f7e499f85e60aac81897a5f
Source noteuspto-grants-2014_02