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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003535Generated: October 27, 2026

Hydrochloric Acid → 2-[N-(2-Sulfoethyl)carbamoyl]-4-(3,4-methylenedioxybenzyl)amino-6-chloroquinazoline hydrochloride

https://huagongshe.com/reaction/1003535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantDiethyl cyanophosphonateHCID 76257—
Reactant2-Carboxy-4-(3,4-methylenedioxybenzyl)amino-6-chloroquinazolineHCID 18796695—
ReactantSodium TaurateHCID 23666486—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-[N-(2-Sulfoethyl)carbamoyl]-4-(3,4-methylenedioxybenzyl)amino-6-chloroquinazoline hydrochlorideHCID 18796792173.8%

Reaction Steps

0.60 ml (3.8 mmol) of diethyl cyanophosphate and 0.90 ml (6.4 mmol) of triethylamine were dropped, in this order, into a solution of 0.50 g (1.4 mmol) of 2-carboxy-4-(3,4-methylenedioxybenzyl)amino-6-chloroquinazoline and 0.28 g (1.9 mmol) of sodium 2-aminoethanesulfonate in 15 ml of dimethylformamide under cooling with ice and stirring. The obtained mixture was stirred at room temperature for several days, followed by the addition of 10 ml of 1N hydrochloric acid and water. The crystals thus precipitated were recovered by filtration, washed with water and air-dried to give 0.61 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046206
Source datasetuspto-grants-2000_04
ORD IDord-cf254ed0d8ec463e94bcfe9638fd8bc5
Source noteuspto-grants-2000_04