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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82795Generated: October 30, 2026

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

https://huagongshe.com/reaction/82795

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-(methoxymethyl)-1,3-thiazol-4-yl]methyl}-2H-1,2,3-triazol-4-amineHCID 67958003—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-(2-((2-(methoxymethyl)thiazol-4-yl)methyl)-2H-1,2,3-triazol-4-yl)-5-phenyloxazole-4-carboxamideHCID 86698197—

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 (42 mg, 0.21 mmol) in CH2Cl2 (3.0 mL) was treated at rt with DMAP (6.6 mg, 0.05 mmol), HOBt (36 mg, 0.26 mmol), EDC (102 mg, 0.53 mmol) and DIPEA (0.16 mL, 0.96 mmol) and the resulting mixture was stirred for 45 min at rt. A solution of 2-((2-(methoxymethyl)thiazol-4-yl)methyl)-2H-1,2,3-triazol-4-amine (48 mg, 0.21 mmol) in CH2Cl2 (3.0 mL) was then added and the reaction mixture was stirred overnight at rt. The mixture was diluted with CH2Cl2 (15.0 mL), the layers were separated and the org. phase was washed with 1N HCl (10.0 mL), water (5.0 mL), followed by brine (10.0 mL) and dried over MgSO4, filtered and the solvents were removed under reduced pressure. Purification of the residue by FC (60:40 hept-EA) gave the title compound as a white solid. TLC: rf (7:3 hept-EA)=0.15. LC-MS-conditions 07: tR=0.83 min, [M+H]+=397.23.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846733B2
Source datasetuspto-grants-2014_09
ORD IDord-5be7842f9e6f4d2399842f466b838ad0
Source noteuspto-grants-2014_09