Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59147Generated: October 29, 2026

HCID 117823909, compound → 2-(6-(((3,3-Difluorocyclobutyl)methoxy)methyl)-2-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenylamino)pyrimidin-4-yl)propan-2-ol

https://huagongshe.com/reaction/59147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 117823909HCID 117823909—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product2-(6-(((3,3-Difluorocyclobutyl)methoxy)methyl)-2-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenylamino)pyrimidin-4-yl)propan-2-olHCID 86344067—

Reaction Steps

Methylmagnesium bromide (0.105 mL, 0.31 mmol) was added to an ice-cold solution of 1-(6-(((3,3-difluorocyclobutyl)methoxy)methyl)-2-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)-phenylamino)pyrimidin-4-yl)ethanone (16 mg, 0.03 mmol) in tetrahydrofuran (5 mL) under argon atmosphere. The mixture was stirred for 10 min. Methylmagnesium bromide (0.058 mL, 0.17 mmol) was added and the mixture was stirred for 10 minutes. The reaction was quenched with of ammonium chloride (aq, sat). The mixture was concentrated. The residue was extracted with dichloromethane. The organic phase was dried over sodium sulfate and concentrated. The residue was purified by preparative HPLC to give the title compound as a dry film (4 mg, 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09439904B2
Source datasetuspto-grants-2016_09
ORD IDord-92980f0133234621864836908c941844
Source noteuspto-grants-2016_09