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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212013Generated: October 30, 2026

Diisopropylethylamine → N-[{(2S)-4-(3,4-Dichlorobenzyl)morpholin-2-yl]methyl}-2-(5-phenyl-2H-tetraazol-2-yl)acetamide

https://huagongshe.com/reaction/2212013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(5-phenyl-2H-1,2,3,4-tetrazol-2-yl)acetic acidHCID 1086563—
Reactant(S)-(4-(3,4-Dichlorobenzyl)morpholin-2-YL)methanamineHCID 10171585—
SolventDimethylformamideHCID 6228—
ProductN-[{(2S)-4-(3,4-Dichlorobenzyl)morpholin-2-yl]methyl}-2-(5-phenyl-2H-tetraazol-2-yl)acetamideHCID 6888355999.8%

Reaction Conditions

Temperature22 °C

Reaction Steps

A solution of (5-phenyl-2H-tetraazol-2-yl)acetic acid (0.082 g) in N,N-dimethylformamide (2 ml) under nitrogen was treated with O-(7-azabenzotriazol-1-yl)-N,N,N′N′-tetramethylammonium hexafluorophosphate (0.152 g) and N,N-diisopropylethylamine (0.139 ml) followed by a solution of Intermediate 9 (0.110 g) in N,N-dimethylformamide (3 ml), and the mixture was stirred at 22° C. for 4 h. The solvent was removed in vacuo and the residue dissolved in ethyl acetate (20 ml). The solution was washed with 10% aqueous citric acid (20 ml), brine (20 ml), saturated aqueous sodium hydrogen carbonate (20 ml) and brine (20 ml), dried (MgSO4) and evaporated in vacuo. Purification by flash chromatography on silica gel (Merck 9385), eluting with ethyl acetate, followed by trituration of the resultant product with diethyl ether, gave the title compound as a white solid (0.184 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101882B2
Source datasetuspto-grants-2006_09
ORD IDord-d4ce371150474eae973372f60c85500e
Source noteuspto-grants-2006_09