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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165295Generated: November 1, 2026

3-Pyridinemethanol → HCID 54273281, compound

https://huagongshe.com/reaction/2165295

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PyridinemethanolHCID 7510—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantHCID 14557735HCID 14557735—
SolventDichloromethaneHCID 6344—
ProductHCID 54273281HCID 54273281—

Reaction Steps

The solution of 2.37 g of N-[4-ethoxycarbonyl-(R*,R*)-2,4-dibenzylbutyryl]-3-aminopropionic acid, 0.61 g of 3-pyridylcarbinol and 1.15 g of dicyclohexylcarbodiimide in 25 ml of methylene chloride is stirred at room temperature for two days. The solid is removed, and the filtrate is diluted with 150 ml of ether and extracted with 0.5N hydrochloric acid. The acidic aqueous layer is separated, basified and extracted with ethyl acetate. The organic layer is washed with saturated sodium chloride, dried over magnesium sulfate, filtered, concentrated and flash chromatographed on silica gel eluting with ethyl acetate:ethanol (9:1) to yield 3-pyridylmethyl N-[4-ethoxycarbonyl-(R*,R*)-2,4-dibenzylbutyryl]-3-aminopropionate as an oil; NMR (CDCl3) δ 8.70 (m, 2H), 7.77 (m, 1H), 7.28 (m, 11H), 5.56 (t, 1H, J=7 Hz), 5.12 (s, 2H), 4.03 (q, 2H, J=8 Hz), 1.08 (t, 3H, J=8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939261
Source datasetuspto-grants-1990_07
ORD IDord-2485b7356940426cb9f0c74d290d88f8
Source noteuspto-grants-1990_07