Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009964Generated: October 30, 2026

Pyridine → HCID 57699908, compound

https://huagongshe.com/reaction/1009964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 57699991HCID 57699991—
SolventDichloromethaneHCID 6344—
ProductHCID 57699908HCID 5769990855.4%

Reaction Steps

To a slurry of N-bromo succinimide (3.54 g, 19.9 mmol) in DCM (30 ml) was added a solution of triphenyl phosphine (4.87 g, 18.8 mmol) in DCM (15 ml). The solution was stirred for a further 5 minutes before addition of pyridine (644 μl, 7.96 mmol) and a solution of (S)-2-tert-Butoxycarbonylamino-5-hydroxy-pentanoic acid cyclopentyl ester (2.0 g, 6.64 mmol) in DCM (20 ml). The solution was stirred for 18 hrs, concentrated in vacuo and the residual solvent azeotroped with toluene (3×30 ml). The residue was triturated with diethyl ether (30 ml) and ethyl acetate:heptane (1:9, 2×30 ml). The combined ether and ethyl acetate/heptane solutions was concentrated onto silica and purified by column chromatography using ethyl acetate/heptane (1:9-2:8) to provide 1.34 g (55% yield) of title compound as a clear oil. 1H NMR (300 MHz, CDCl3), δ 5.25 (1 H, m), 5.05 (1H, bd), 3.45 (2H, m), 2.00-1.55 (12H, bm), 1.45 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973181B2
Source datasetuspto-grants-2011_07
ORD IDord-09277e9cbaef43fda54ba2f9622b4082
Source noteuspto-grants-2011_07