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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82852Generated: October 29, 2026

1,2-Dichloroethane → N-(2-((4-(Methoxymethyl)oxazol-2-yl)methyl)-2H-1,2,3-triazol-4-yl)-2-methyl-5-(m-tolyl)oxazole-4-carboxamide

https://huagongshe.com/reaction/82852

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantNitrogenHCID 947—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Methyl-5-(m-tolyl)oxazole-4-carboxylic acidHCID 66929205—
ReactantHCID 67958086HCID 67958086—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-(2-((4-(Methoxymethyl)oxazol-2-yl)methyl)-2H-1,2,3-triazol-4-yl)-2-methyl-5-(m-tolyl)oxazole-4-carboxamideHCID 57336777—

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 2-methyl-5-(m-tolyl)oxazole-4-carboxylic acid (WO 2009/077990, p. 112) (1.14 g, 5.26 mmol) in CH2Cl2 (30 mL) was treated at rt with DMAP (160 mg, 1.31 mmol), HOBt (854 mg, 6.32 mmol), EDC (2.52 g, 13.15 mmol) and DIPEA (3.60 mL, 21.03 mmol) and the resulting mixture was stirred for 45 min at rt. A solution of 2-((4-(methoxymethyl)oxazol-2-yl)methyl)-2H-1,2,3-triazol-4-amine (1.10 g, 5.26 mmol) in CH2Cl2 (22 mL) was then added and the reaction mixture was stirred overnight at rt. The mixture was diluted with CH2Cl2 (45 mL), the layers were separated and the org. phase was washed with water (45 mL), dried over MgSO4, filtered and the solvents were removed under reduced pressure. Purification of the residue by FC (4:6 hept-EA) gave the title compound as a colorless oil: TLC: rf (4:6 hept-EA)=0.20. LC-MS-conditions 07: tR=0.88 min, [M+H]+=409.11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846733B2
Source datasetuspto-grants-2014_09
ORD IDord-56c2699a94ae41908321b288acf9e9d0
Source noteuspto-grants-2014_09