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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405946Generated: October 31, 2026

Sodium Bicarbonate → HCID 68155180, compound

https://huagongshe.com/reaction/1405946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
Reactant(5-(4-(4-((3-Fluorobenzyl)oxy)-3-chloroanilino)-6-quinazolinyl)-2-furancarboxaldehydeHCID 11181296—
ReactantN-(2-aminoethyl)methanesulfonamide hydrochlorideHCID 22609809—
SolventTriethylamineHCID 8471—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 68155180HCID 6815518045%

Reaction Conditions

Temperature0 °C

Reaction Steps

At room temperature, 10.0 g of compound 5-(4-(4-(3-fluorobenzyloxy)-3-chloroanilino)-6-quinazolinyl)furan-2-formaldehyde, 6.5 g of compound N-(2-aminoethyl)methanesulfonamide hydrochloride, and 14.6 g of triethylamine in the mixture of dichloromethane/methanol (3:1) were stirred overnight, then cooled with ice-bath to 0° C., and 1.4 g of sodium borohydride was added at that temperature. The mixture was warmed to room temperature, stirred overnight, saturated sodium bicarbonate was added to quench the reaction, and extracted with ethyl acetate. The organic phase was washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate, and subjected to a column chromatography to obtain 5.7 g of the desired product, yield 45.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916574B2
Source datasetuspto-grants-2014_12
ORD IDord-a58cb3cc806146349e7a0c0423e309f7
Source noteuspto-grants-2014_12