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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306740Generated: October 26, 2026

Hydrochloric Acid → HCID 17885200, compound

https://huagongshe.com/reaction/2306740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Aminoethanesulphonamide monohydrochlorideHCID 3021549—
Reactant5-(4-(4-Benzyloxy-phenylamino)-quinazolin-6-yl)-furan-2-carbaldehyde hydrochlorideHCID 21952306—
CatalystTriethylamineHCID 8471—
SolventWaterHCID 962—
ProductHCID 17885200HCID 1788520037%

Reaction Steps

In an analogous manner to Example 10, 5-(4-(4-Benzyloxy-phenylamino)-quinazolin-6-yl)-furan-2-carbaldehyde hydrochloride (0.200 g, 0.436 mmol) was reacted with 2-aminoethylsulphonamide hydrochloride (0.200 g, 1.245 mmol) and triethylamine (10 drops). On completion of the reaction, the mixture was acidified with dilute HCl and diluted with water, to give the crude product as a precipitate collected by filtration. Treatment with triethylamine followed by purification by silica gel chromatography, eluting with 3-10% MeOH/CHCl3 gave the title compound as a yellow solid (0.085 g, 0.160 mmol, 37%); δH [2H6]DMSO 9.61 (2H, brs), 9.25 (1H, s), 8.58 (1H, s), 8.23 (1H, d), 7.77-7.88 (3H, m), 7.30-7.52 (5H, m), 7.26 (2H, s), 7.20 (1H, d), 7.08 (2H, d), 6.81 (1H, d), 5.14 (2H, s), 4.44 (2H, s), 3.34-3.60 (2H, m), 3.25-3.45 (2H,obscured by water); m/z (M+1+) 530.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06828320B2
Source datasetuspto-grants-2004_12
ORD IDord-3e700ee264e84035b14c26c50f21a3fe
Source noteuspto-grants-2004_12