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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631123Generated: November 3, 2026

Water → 2-{2-[2-Amino-4-(1,3-dihydroisoindole-2-carbonyl)quinazolin-6-yl]benzylamino}acetamide

https://huagongshe.com/reaction/1631123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantGlycinamide hydrochlorideHCID 2723639—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-[2-Amino-4-(1,3-dihydroisoindole-2-carbonyl)quinazolin-6-yl]benzaldehydeHCID 59483516—
Solvent1,2-DichloroethaneHCID 11—
SolventTetrahydrofuranHCID 8028—
Product2-{2-[2-Amino-4-(1,3-dihydroisoindole-2-carbonyl)quinazolin-6-yl]benzylamino}acetamideHCID 56943543—

Reaction Conditions

Temperature60 °C

Reaction Steps

100 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. 39 mg of aminoacetamide hydrochloride are added, and the mixture is stirred at 60° C. for 6 h. After cooling to 25° C., 113 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-2c7586b32ab74fd2af71dee9a1bce016
Source noteuspto-grants-2014_07