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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503672Generated: November 3, 2026

Hydrochloric Acid → HCID 16115123, compound

https://huagongshe.com/reaction/503672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolamineHCID 700—
ReactantHCID 16115119HCID 16115119—
CatalystDimethylformamideHCID 6228—
SolventThionyl ChlorideHCID 24386—
ProductHCID 16115123HCID 1611512382.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 8 (3.20 g, 6.79 mmol) in SOCl2 (60 mL) containing DMF (2 drops) was heated under reflux for 1 h. Evaporation of the solvent under reduced pressure, followed by azeotroping in with benzene gave the crude acid chloride, which was dissolved in dry Me2CO (80 mL) and treated at 0° C. with 2-aminoethanol (1.24 g, 20.3 mmol). After stirring at 0° C. for 5 min, the mixture was acidified to pH 2-3 with 0.2 N HCl, concentrated to half volume, and then solid NaBr was added. The mixture was extracted with EtOAc (2×) and the combined extracts were washed with saturated NaBr solution, dried (Na2SO4) and evaporated. The residue was chromatographed on silica gel, eluting with EtOAc/MeOH (15:1) to give 2-(5-{[(2-hydroxyethyl)amino]carbonyl} {2-[(methylsulfonyl)oxy]ethyl}-2,4-dinitroanilino)ethyl methanesulfonate (9a) (2.87 g, 82%) as a gum that was used directly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776924B2
Source datasetuspto-grants-2010_08
ORD IDord-c81f37b4aa2f490b8fe76ad4429e3412
Source noteuspto-grants-2010_08