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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82798Generated: October 30, 2026

1,2-Dichloroethane → N-(2-((2-(2-methoxypropan-2-yl)oxazol-4-yl)methyl)-2H-1,2,3-triazol-4-yl)-5-phenyloxazole-4-carboxamide

https://huagongshe.com/reaction/82798

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantNitrogenHCID 947—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Phenyl-1,3-oxazole-4-carboxylic acidHCID 2776299—
Reactant2-((2-(2-methoxypropan-2-yl)oxazol-4-yl)methyl)-2H-1,2,3-triazol-4-amineHCID 67957927—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-(2-((2-(2-methoxypropan-2-yl)oxazol-4-yl)methyl)-2H-1,2,3-triazol-4-yl)-5-phenyloxazole-4-carboxamideHCID 86698200—

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of commercially available 5-phenyloxazole-4-carboxylic acid (18 mg, 0.10 mmol) in CH2Cl2 (1.0 mL) was treated at rt with DMAP (3.0 mg, 0.02 mmol), HOBt (15.7 mg, 0.12 mmol), EDC (46.5 mg, 0.24 mmol) and DIPEA (0.07 mL, 0.39 mmol) and the resulting mixture was stirred for 45 min at rt. A solution of 2-((2-(2-methoxypropan-2-yl)oxazol-4-yl)methyl)-2H-1,2,3-triazol-4-amine (23.0 mg, 0.10 mmol) in CH2Cl2 (0.5 mL) was then added and the reaction mixture was stirred overnight at rt. The mixture was diluted with CH2Cl2 (10.0 mL), the layers were separated and the org. phase was washed with water (5.0 mL), dried over MgSO4, filtered and the solvents were removed under reduced pressure. Purification of the residue by FC (50:50 hept-EA) gave the title compound as a yellow oil. TLC: rf (50:50 hept-EA)=0.27. LC-MS-conditions 07: tR=0.86 min, [M+H]+=408.89.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846733B2
Source datasetuspto-grants-2014_09
ORD IDord-84def6b3586b457b869c3ccc1d42af47
Source noteuspto-grants-2014_09