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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527249Generated: October 30, 2026

Hydrochloric Acid → HCID 57377975, compound

https://huagongshe.com/reaction/527249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantNitrogenHCID 947—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylaluminumHCID 16682925—
ReactantN-(2-((4-acetyloxazol-2-yl)methyl)-2H-1,2,3-triazol-4-yl)-2-methyl-5-(m-tolyl)oxazole-4-carboxamideHCID 67967926—
SolventDichloromethaneHCID 6344—
SolventHeptaneHCID 8900—
ProductHCID 57377975HCID 57377975—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of N-(2-((4-acetyloxazol-2-yl)methyl)-2H-1,2,3-triazol-4-yl)-2-methyl-5-(m-tolyl)oxazole-4-carboxamide (622 mg, 1.53 mmol) in CH2Cl2 (15 mL) was treated at 0° C. with AlMe3 (2.3 mL of a 2.0M solution in heptane, 4.6 mmol) and the resulting mixture was stirred for 2 h at 0° C. The reaction mixture was carefully poured into a sat. aq. solution of ammonium chloride (10 mL) and diluted with CH2Cl2 (20 mL). 1N HCl (10 mL) was then added. The layers were separated and the org. phase was dried over Na2SO4, filtered and the solvents were removed under reduced pressure. Purification of the residue by FC (3:7 hept-EA) gave the title compound as a white solid: TLC: rf (3:7 hept-EA)=0.28. LC-MS-conditions 06: tR=0.85 min, [M+H]+=423.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346793B2
Source datasetuspto-grants-2016_05
ORD IDord-a3c38e95410340279dc2bc41cf2c8517
Source noteuspto-grants-2016_05