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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82790Generated: October 26, 2026

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

https://huagongshe.com/reaction/82790

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—
Reactant2-((2-(methoxymethyl)thiazol-5-yl)methyl)-2H-1,2,3-triazol-4-amineHCID 67958100—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-(2-((2-(Methoxymethyl)thiazol-5-yl)methyl)-2H-1,2,3-triazol-4-yl)-2-methyl-5-(m-tolyl)oxazole-4-carboxamideHCID 67968178—

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) (70.0 mg, 0.32 mmol) in CH2Cl2 (1.5 mL) was treated at rt with DMAP (9.8 mg, 0.08 mmol), HOBt (52 mg, 0.39 mmol), EDC (154 mg, 0.81 mmol) and DIPEA (0.22 mL, 1.3 mmol) and the resulting mixture was stirred for 30 min at rt. A solution of 2-((2-(methoxymethyl)thiazol-5-yl)methyl)-2H-1,2,3-triazol-4-amine (73 mg, 0.32 mmol) in CH2Cl2 (1.5 mL) was then added and the reaction mixture was stirred overnight at rt. The mixture was diluted with CH2Cl2 (5.0 mL), the layers were separated and the org. phase was washed with water (5.0 mL) dried over Na2SO4, 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)=0.29. LC-MS-conditions 07: tR=0.94 min, [M+H]+=425.09.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846733B2
Source datasetuspto-grants-2014_09
ORD IDord-ef29e5e15e4d4eb08e1419593a2ad64f
Source noteuspto-grants-2014_09