Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450724Generated: November 1, 2026

Hydrochloric Acid → HCID 178460133, compound

https://huagongshe.com/reaction/450724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantDiisopropylethylamineHCID 81531—
ReactantPropionylglycineHCID 98681—
ReactantHOAtHCID 181649—
ReactantHCID 67023917HCID 67023917—
SolventDimethylformamideHCID 6228—
ProductHCID 178460133HCID 17846013361%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of N-(3,4-diamino-phenyl)-4-isopropyl-benzenesulfonamide×HCl (500 mg, 1.32 mmol) in DMF (20 ml) at 0° C. was added propionylamino-acetic acid (170 mg, 1.32 mmol) and 1-hydroxy-7-azabenzotriazole (HOAt) (220 mg, 1.59 mmol). After stirring the mixture at 0° C. for 15 min EDC (N-ethyl-N′-(3-dimethylaminopropyl)-carbodiimide) (300 mg, 1.45 mmol) was added. DIPEA (diisopropylethylamine) (0.92 ml, 5.29 mmol) was added after stirring another 15 min at 0° C. The mixture was stirred at room temperature for 16 h, and then concentrated under reduced pressure. The residue was partitioned between ethyl acetate and saturated aqueous NaHCO3 and the organic layer was dried over MgSO4, filtered, and the solvent evaporated under reduced pressure. A solution of the obtained oil in acetic acid was heated to 70° C. for 6 h. After evaporation of the solvent in vacuo the residue was purified by column chromatography to give the product as a yellow oil (320 mg, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486984B2
Source datasetuspto-grants-2013_07
ORD IDord-8d9ad607050c481cb04f0423e2542194
Source noteuspto-grants-2013_07