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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857758Generated: October 30, 2026

1,2-Dichloroethane → HCID 58760139, compound

https://huagongshe.com/reaction/857758

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDimethylformamideHCID 6228—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantN-[5-chloro-2-(1H-tetraazol-1-yl)benzyl]-L-prolinamideHCID 69655818—
ProductHCID 58760139HCID 58760139—

Reaction Steps

To a solution of R-mandelic acid (60 mg, 0.39 mmol), N-[5-chloro-2-(1H-tetraazol-1-yl)benzyl]-L-prolinamide (Example 26, Step B, 120 mg, 0.39 mmol, HPLC RT=2.25 min, method A), and HOBt hydrate (60 mg, 0.39 mmol) in DMF (3 mL) was added EDC (98 mg, 0.51 mmol). Diisopropylethylamine was then added slowly in portions (˜0.05 mL total) to bring the pH of the solution to 6–7 as measured on wetted E. Merck pH indicator strips. The mixture was stirred at ambient temperature for 18 h, and the solvent was removed under reduced pressure. The residue was partitioned between EtOAc (50 mL) and saturated aqueous NaHCO3 (10 mL). The EtOAc layer was separated, dried over anhydrous MgSO4, and filtered. The filtrate solvent was removed under reduced pressure and the residue was purified by pressurized silica gel column chromatography using EtOAc as eluant. Product-containing fractions were combined and the solvent was removed under reduced pressure to give the title compound as an amorphous solid (TLC Rf=0.6 (EtOAc); HPLC RT=2.82 min, method A; LCMS m/z=441).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144899B2
Source datasetuspto-grants-2006_12
ORD IDord-af0357fa4f2549acbc445f07925b96da
Source noteuspto-grants-2006_12