HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392238Generated: October 25, 2026
[4-(4-[1,2,3]Triazol-1-yl-butyl)phenyl]-carbamic acid tert-butyl ester → [4-(4-[1,2,3]Triazol-1-yl-butyl)-phenyl]-[2-(5-trifluoromethoxy-1H-indol-2-yl)-oxazol-4-ylmethyl]-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/1392238
Participants
| Role | Name | HCID | Charge |
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| Reactant | [4-(4-[1,2,3]Triazol-1-yl-butyl)phenyl]-carbamic acid tert-butyl ester | HCID 69220256 | — |
| Reactant | 2-(4-chloromethyl-oxazol-2-yl)-5-trifluoromethoxy-1H-indole | HCID 136331965 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [4-(4-[1,2,3]Triazol-1-yl-butyl)-phenyl]-[2-(5-trifluoromethoxy-1H-indol-2-yl)-oxazol-4-ylmethyl]-carbamic acid tert-butyl ester | HCID 136331972 | — |
Reaction Steps
To a solution of [4-(4-[1,2,3]Triazol-1-yl-butyl)-phenyl]-carbamic acid tert-butyl ester (0.297 g, 0.94 mmol) in N,N-dimethyl formamide (5 ml) sodium hydride (0.050 g, 2.1 mmol) was added and the mixture stirred for 30 min at r.t. To this mixture a solution of 2-(4-chloromethyl-oxazol-2-yl)-5-trifluoromethoxy-1H-indole 0.3 g, 0.94 mmol) in N,N-dimethyl formamide (5 ml) was added and stirring continued for 16 h. The mixture was then poured on water (25 ml) and extracted with ethyl acetate (3×25 ml). The combined organic extracts was washed with water, brine and dried over sodium sulfate. After concentration in vacuo the crude product was purified on silica gel (iso-hexanes/ethyl acetate 1:2) to yield [4-(4-[1,2,3]Triazol-1-yl-butyl)-phenyl]-[2-(5-trifluoromethoxy-1H-indol-2-yl)-oxazol-4-ylmethyl]-carbamic acid tert-butyl ester as light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07342030B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-5b5133160aae44da964fa3395110c878 |
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| Source note | uspto-grants-2008_03 |
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