Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076326Generated: October 30, 2026

Acetic Acid → HCID 67095880, compound

https://huagongshe.com/reaction/2076326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 178513278HCID 178513278—
SolventAcetonitrileHCID 6342—
ProductHCID 67095880HCID 6709588026.9%

Reaction Steps

To a stirred solution of acetic acid (127 mg, 2.12 mmol) in acetonitrile (8.5 ml) was added at room temperature 1-hydroxy-benzotriazole (403 mg, 2.98 mmol) and N-(3-dimethylaminopropyl)-N′-ethyl-carbodiimid-hydrochloride (465 mg, 2.43 mmol). The mixture was allowed to stir for 3 h at room temperature and N-hydroxy-2-((R)-indan-1-ylamino)-quinoline-5-carboxamidine (450 mg, 1.41 mmol) was added together with acetonitrile (7.5 ml). The mixture was allowed to stir for 2 h at room temperature, evaporated to dryness and diluted with acetic acid (14 ml). The reaction mixture was allowed to stir for 2 h at 100° C., evaporated, poured into saturated NaHCO3 solution (50 ml) and extracted with ethyl acetate (3×80 ml). The combined organic layers were washed with brine (2×50 ml), dried (MgSO4) and evaporated. The crude product was purified by flash chromatography (ethyl acetate/heptane) on silica gel and crystallization (ethyl acetate/heptane) to yield the title compound as light yellow solid (130 mg, 18%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923561B2
Source datasetuspto-grants-2011_04
ORD IDord-e24e0704680f4ee5a91a798f981fde88
Source noteuspto-grants-2011_04