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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416645Generated: October 29, 2026

Diisopropylethylamine → HCID 86759568, compound

https://huagongshe.com/reaction/2416645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantBoc-3-(2-pyridyl)-Ala-OHHCID 2734482—
ReactantO-benzylglycine toluene-p-sulphonateHCID 6451311—
SolventDimethylformamideHCID 6228—
ProductHCID 86759568HCID 8675956890.6%

Reaction Steps

To a solution of (2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-pyridyl)propanoic acid (55.0 g), glycine benzyl ester tosylate (69.7 g), and diphenylphosphoryl azide (46.7 ml) in N,N-dimethylformamide (550 ml) was added dropwise N,N-diisopropylethylamine (75.6 ml) at 4° C. The mixture was warmed to room temperature and stirred for 3 hours. The resulting mixture was poured into ice-cold saturated aqueous sodium hydrogencarbonate solution (700 ml). The mixture was extracted twice with ethyl acetate (total 1.3 L) and washed successively with water (400 ml×2), saturated aqueous ammonium chloride solution (200 ml), aqueous sodium hydrogencarbonate solution (300 ml×2), and brine (40 ml). The organic layer was dried over anhydrous magnesium sulfate and concentrated to give the title compound (77.4 g) as pale brown crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825200B1
Source datasetuspto-grants-2004_11
ORD IDord-aee862d091884d789cd7a378dfc12955
Source noteuspto-grants-2004_11