Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 86664915 | HCID 86664915 | — |
| Reactant | 2-[5-(2-Methyl-[1,3]dioxolan-2-yl)-thiophen-2-ylmethyl]-oxazole-4-carbonyl chloride | HCID 86664916 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86664913 | HCID 86664913 | — |
| Product | 2-[5-(2-Methyl-[1,3]dioxolan-2-yl)-thiophen-2-ylmethyl]-oxazole-4-carbonyl azide | HCID 86664914 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08674111B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-bacd367fd2754ddabc7bf3fd4606ec8d |
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| Source note | uspto-grants-2014_03 |
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