Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721469Generated: November 2, 2026

4-Aminosalicylic Acid → HCID 86748782, compound

https://huagongshe.com/reaction/1721469

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminosalicylic AcidHCID 4649—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantPhosphorus oxide (P4O10)HCID 14812—
ReactantN-HydroxysuccinimideHCID 80170—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86748782HCID 86748782—

Reaction Steps

4-Amino salicylic acid (2.07 g, 13 mM), N-hydroxy-succinimide (2.07 g, 18 mmol) and DCC (3.44 g, 19 mmol), which had been dried over night over phosphorus pentoxide in vacuum, were dissolved sequentially in anhy. tetrahydrofuran (150 mL) in a round bottom flask. A vacuum was then applied for 30 seconds, the flask sealed and the reaction allowed to proceed for 7 hours at 1°-0° C., maintaining continuous stirring. After this time, the solvent was removed under vacuum and the residue re-dissolved in 15 mL CHCl3 /acetonitrile (CH3CN) (98:2). This solution was chromatographed using 80 g silica gel, eluting sequentially with 300 mL each, CHCl3 /CH3CN (95:5), CHCl3 /CH3CN (90:10) and CHCl3 /CH3CN (50:50). HASA began eluting in the tail end of CHCl3 /CH3CN (95:5) and continued throughout the elution with 10% CH3CN. A total of 2.4 g (70%) of purified HASA (XXXII) was obtained, Rf =0.64 (CHCl3 /CH3CN, 20.3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05510500
Source datasetuspto-grants-1996_04
ORD IDord-b7a79fe9ff9d419bb98df8ebdb67f4a7
Source noteuspto-grants-1996_04