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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631125Generated: November 3, 2026

Acetic Acid → HCID 56943574, compound

https://huagongshe.com/reaction/1631125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCyclobutylamineHCID 75645—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-[2-Amino-4-(1,3-dihydroisoindole-2-carbonyl)quinazolin-6-yl]benzaldehydeHCID 59483516—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 56943574HCID 56943574—

Reaction Conditions

Temperature60 °C

Reaction Steps

200 mg of 2-[2-amino-4-(1,3-dihydroisoindole-2-carbonyl)quinazolin-6-yl]benzaldehyde are dissolved in 3 ml of 1,2-dichloroethane and 3 ml of tetrahydrofuran. 106 μl of cyclobutylamine and 35 μl of glacial acetic acid are added, and the mixture is stirred at 60° C. for 6 h. After cooling to 25° C., 226 mg of sodium triacetoxyborohydride are added and stirred at 25° C. for a further 12 h. The mixture is poured into water, extracted three times with dichloromethane, and the combined organic phases are dried over sodium sulfate. After filtration, the filtrate is evaporated to dryness and purified by chromatography (reversed phase HPLC).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791129B2
Source datasetuspto-grants-2014_07
ORD IDord-5da06a7e7a814b92b007bc94d42a7472
Source noteuspto-grants-2014_07