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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246206Generated: November 1, 2026

Pyridine → HCID 45092039, compound

https://huagongshe.com/reaction/1246206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantCyanuric fluorideHCID 12664—
Reactant(S)-2-((tert)-Butoxycarbonyl)amino)butanoic acidHCID 2755934—
SolventDichloromethaneHCID 6344—
ProductHCID 45092039HCID 45092039111.6%

Reaction Steps

(S)-2-(Tert-butoxycarbonylamino)butyric acid (0.010 mol) dissolved in DCM (25 ml) was placed in a cooling bath at −10° C. Pyridine (0.010 mol) was added, followed by 2,4,6-trifluoro-1,3,5-triazine (0.0345 mol). The mixture was stirred under nitrogen. After one hour, ice cold water (75 ml) was added. More DCM (45 ml) was added, and the mixture was shaken. The organic phase was separated, washed with ice cold water again (100 ml), then the organic phase dried, filtered, and concentrated to yield 2.29 g of (S)-1,1-dimethylethyl [1-(fluorocarbonyl)propyl]-carbamate (intermediate 25).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125891B2
Source datasetuspto-grants-2006_10
ORD IDord-b34a80d2c9a34178ba71ab3cf2c1fdea
Source noteuspto-grants-2006_10