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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189403Generated: October 30, 2026

Nitrogen → HCID 86664913, compound

https://huagongshe.com/reaction/1189403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantSodium AzideHCID 33557—
ReactantHCID 86664915HCID 86664915—
Reactant2-[5-(2-Methyl-[1,3]dioxolan-2-yl)-thiophen-2-ylmethyl]-oxazole-4-carbonyl chlorideHCID 86664916—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 86664913HCID 86664913—
Product2-[5-(2-Methyl-[1,3]dioxolan-2-yl)-thiophen-2-ylmethyl]-oxazole-4-carbonyl azideHCID 86664914—

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 this crude mixture of 2-(5-acetyl-thiophen-2-ylmethyl)-oxazole-4-carbonyl chloride and 2-[5-(2-methyl-[1,3]dioxolan-2-yl)-thiophen-2-ylmethyl]-oxazole-4-carbonyl chloride in dry acetone (12.0 mL) was cooled to 0° C. and a solution of sodium azide (262 mg, 3.98 mmol) in H2O (1.4 mL) was added over 1 h. The reaction mixture was stirred at 0° C. for 45 min. The mixture was concentrated under reduced pressure (co-evaporation with toluene) then dissolved in CH2Cl2 and filtered. The filtrated was concentrated under reduced pressure to give the title compound (LC-MS-conditions 01: tR=0.85 min, [M+H]+=276.91) along with 2-[5-(2-methyl-[1,3]dioxolan-2-yl)-thiophen-2-ylmethyl]-oxazole-4-carbonyl azide (LC-MS-conditions 01: tR=0.91 min, [M+H]+=320.92) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674111B2
Source datasetuspto-grants-2014_03
ORD IDord-bacd367fd2754ddabc7bf3fd4606ec8d
Source noteuspto-grants-2014_03