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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631181Generated: October 27, 2026

Tetra-n-butylammonium di-tert-butylphosphate → [2-[2-Amino-4-(isoindoline-2-carbonyl)quinazolin-6-yl]-4,5-difluorophenyl]methyl di-tert-butyl phosphate

https://huagongshe.com/reaction/1631181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetra-n-butylammonium di-tert-butylphosphateHCID 22339116—
Reactant[2-Amino-6-(2-chloromethyl-4,5-difluorophenyl)quinazolin-4-yl]-(1,3-dihydroisoindol-2-yl)methanoneHCID 66837605—
SolventAcetonitrileHCID 6342—
Product[2-[2-Amino-4-(isoindoline-2-carbonyl)quinazolin-6-yl]-4,5-difluorophenyl]methyl di-tert-butyl phosphateHCID 66836649—

Reaction Conditions

Temperature80 °C

Reaction Steps

800 mg of tetrabutylammonium di-tert-butylphosphate are added to 270 mg of [2-amino-6-(2-chloromethyl-4,5-difluorophenyl)quinazolin-4-yl]-(1,3-dihydroisoindol-2-yl)methanone dissolved in 20 ml of acetonitrile, and the solution obtained is heated at 80° C. for 2 h. After cooling to 25° C., undissolved material is filtered off, and the filtrate is evaporated to dryness in vacuo. The residue is dissolved in 1 ml of dimethyl sulfoxide and purified by chromatography (reversed phase).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791129B2
Source datasetuspto-grants-2014_07
ORD IDord-44a1641c3abb4f5384e7ba77deb27cf0
Source noteuspto-grants-2014_07