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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetra-n-butylammonium di-tert-butylphosphate | HCID 22339116 | — |
| Reactant | [2-Amino-6-(2-chloromethyl-4,5-difluorophenyl)quinazolin-4-yl]-(1,3-dihydroisoindol-2-yl)methanone | HCID 66837605 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | [2-[2-Amino-4-(isoindoline-2-carbonyl)quinazolin-6-yl]-4,5-difluorophenyl]methyl di-tert-butyl phosphate | HCID 66836649 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08791129B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-44a1641c3abb4f5384e7ba77deb27cf0 |
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| Source note | uspto-grants-2014_07 |
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