HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271440Generated: November 2, 2026
Sodium hydride → [4-(4-[1,2,3]Triazol-1-yl-but-1-enyl)-phenyl]-{2-[2-(4-trifluoromethane-sulfinyl-phenyl)-vinyl]-oxazol-4-ylmethyl}-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/1271440
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Chloromethyl-2-[2-(4-trifluoromethylsulfinyl-phenyl)-vinyl]-oxazole | HCID 69292389 | — |
| Reactant | [4-(4-[1,2,3]Triazol-1-yl-but-1-enyl)-phenyl]-carbamic acid tert-butyl ester | HCID 69490216 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [4-(4-[1,2,3]Triazol-1-yl-but-1-enyl)-phenyl]-{2-[2-(4-trifluoromethane-sulfinyl-phenyl)-vinyl]-oxazol-4-ylmethyl}-carbamic acid tert-butyl ester | HCID 69489717 | 91.3% |
Reaction Steps
A solution of [4-(4-[1,2,3]triazol-1-yl-but-1-enyl)-phenyl]-carbamic acid tert-butyl ester (0.157 g, 0.5 mmol) in N,N-dimethyl formamide (4 ml) was treated with sodium hydride (0.014 g, 0.5 mmol) and stirred for 30 min at room temperature. After addition of 4-chloromethyl-2-[2-(4-trifluoromethanesulfinyl-phenyl)-vinyl]-oxazole (0.168 g, 0.5 mmol) and stirring for 12 h the reaction was quenched by the addition of a sat. NH4Cl solution (8 ml). Extraction with ethyl acetate (3×10 ml), washing with water, drying over sodium sulfate and concentration in vacuo yields crude [4-(4-[1,2,3]triazol-1-yl-but-1-enyl)-phenyl]-{2-[2-(4-trifluoromethane-sulfinyl-phenyl)-vinyl]-oxazol-4-ylmethyl}-carbamic acid tert-butyl ester (0.28 g) which was used in the next step without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07205326B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-82661148720549cdbb309e3d4236078c |
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| Source note | uspto-grants-2007_04 |
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