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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540418Generated: October 30, 2026

Triethylamine → HCID 178450010, compound

https://huagongshe.com/reaction/540418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant(R)-2-amino-1-(3-butoxy-3-o-tolylazetidin-1-yl)-3-(4-methoxyphenyl)propan-1-one hydrochlorideHCID 66988286—
ReactantHCID 178525822HCID 178525822—
SolventDimethylformamideHCID 6228—
ProductHCID 178450010HCID 17845001013%

Reaction Steps

0.1 ml (0.8 mmol) of triethylamine is added to a solution containing 50 mg (0.3 mmol) of (S)-2-hydroxy-3-(1H-imidazol-4-yl)propanoic acid and 100 mg (0.3 mmol) of TBTU in 2 ml of dimethylformamide. After stirring for 1 hour at ambient temperature, 128 mg (0.3 mmol) of (R)-2-amino-1-(3-butoxy-3-o-tolyl-azetidin-1-yl)-3-(4-methoxyphenyl)propan-1-one hydro-chloride (described in Example 6.2) are added and the mixture is stirred for 72 h at ambient temperature. A 1N aqueous solution of sodium hydroxide is added and the medium is extracted with a 20/80 heptane/ethyl acetate mixture. The organic phase is dried over magnesium sulphate, filtered and concentrated. The crude product is purified by preparative thin layer chromatography (eluent: 90/10 dichloro-methane/methanol). 17 mg of (S)—N—[(R)-2-(3-butoxy-3-o-tolylazetidin-1-yl)-1-(4-methoxybenzyl)-2-oxoethyl]-2-hydroxy-3-(1H-imidazol-4-yl)propionamide are obtained in the form of a white powder with a yield of 13%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871187B2
Source datasetuspto-grants-2014_10
ORD IDord-1c84c1bd1a514fbda709b74b9eb704f3
Source noteuspto-grants-2014_10