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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57727Generated: October 24, 2026

Diisopropylethylamine → 3-(2-Benzyloxy-propionylamino)-3H-imidazole-4-carboxylic acid methyl ester

https://huagongshe.com/en/reaction/57727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(Benzyloxy)propanoic acidHCID 245987—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant3-(2-Benzyloxy-acetylamino)-3H-imidazole-4-carboxylic acid methyl esterHCID 89715196—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Benzyloxy-propionylamino)-3H-imidazole-4-carboxylic acid methyl esterHCID 8971519591%

Reaction Steps

To a solution of compound 2 (4.2 g, 29.7 mmol), 2-Benzyloxy-propionic acid (5.5 g, 29.7 mmol) and DIEA (10 mL) in a mixture of DMF (1 mL) and THF (50 mL) in ice-water bath was added HATU (13.5 g, 35.7 mmol). The resulting mixture was then stirred at ambient temperature overnight. Water (100 mL) was added. The mixture was extracted with ethyl acetate (300 mL×2). The combined organic phases were concentrated to give a crude residue, which was purified by chromatography on silica gel column (eluted with PE/EtOAc=1:1 to 1:3) to afford compound 9 (8.2 g, 91% yield) as brown oil. LC-MS: m/z 304 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434733B2
Source datasetuspto-grants-2016_09
ORD IDord-efc87d032fbe4100bf345dd07e40e300
Source noteuspto-grants-2016_09