Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592054Generated: November 3, 2026

Pyridine → HCID 117717655, compound

https://huagongshe.com/reaction/592054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantHCID 89738579HCID 89738579—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 117717655HCID 11771765595%

Reaction Steps

(1S,2R,3S,4R)-3-(tert-butoxycarbonylamino)-7-oxabicyclo[2.2.1]heptane-2-carboxylic acid (13) (44 mg, 0.17 mmol) was taken in dioxane when pyridine (1.7 eq) was added followed by addition of BOC2O. The reaction mixture was stirred at rt for 40 min when NH4CO3 (38 mg, 0.49 mmol) was added and the reaction mixture was stirred at rt for 15 h when TLC confirmed formation of product. The reaction mixture was concentrated and purified by column chromatography using silica gel (100-200 mesh) to afford the desired product (43 mg, 95%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238656B2
Source datasetuspto-grants-2016_01
ORD IDord-63476d7664c644079bf401444660bb95
Source noteuspto-grants-2016_01