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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824670Generated: October 31, 2026

Pyridine → HCID 11458610, compound

https://huagongshe.com/reaction/1824670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantCyanuric fluorideHCID 12664—
Reactant(2R)-1-[(tert-butoxy)carbonyl]pyrrolidine-2-carboxylic acidHCID 688022—
SolventDichloromethaneHCID 6344—
ProductHCID 11458610HCID 11458610—

Reaction Conditions

Temperature-15 °C

Reaction Steps

To an oven-dried, septaed 10 mL round-bottom flask, cooled under an argon atmosphere, and charged with (R)-N-BOC-proline, 24d, (215.3 mg, 1.00 mmol) was added 2.5 mL freshly distilled CH2Cl2 under argon. The reaction was cooled to −15° C. and to the flask was added cyanuric fluoride (450 μL, 5 mmol). The reaction was stirred at −15° C. for 15 minutes then anhydrous pyridine (81 μL, 1.0 mmol) was added. Stirring was maintained at −15° C. for 90 minutes. Without warming, the crude reaction was poured over ice, and immediately extracted twice with CH2Cl2. The combined CH2Cl2 extracts were washed once with water, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to afford 170.3 mg of 25d as a colorless oil. FTIR (neat) 1850 cm−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045360B2
Source datasetuspto-grants-2006_05
ORD IDord-2c259698fe78455ea172f6100d2c77c3
Source noteuspto-grants-2006_05