HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775325Generated: October 25, 2026
tert-Butyl piperazine-1-carboxylate → tert-Butyl 4-(4-methylthiazol-5-yl)piperazine-1-carboxylate
https://huagongshe.com/reaction/1775325
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 5-Bromo-4-methyl-1,3-thiazole | HCID 15020997 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Catalyst | Brettphos | HCID 25112535 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | tert-Butyl 4-(4-methylthiazol-5-yl)piperazine-1-carboxylate | HCID 89825959 | 207.6% |
Reaction Steps
A solution of 5-bromo-4-methylthiazole (454 mg, 2.55 mmol), N-Boc-piperazine (940 mg, 5.05 mmol), sodium tert-butoxide (492 mg, 5.12 mmol) and dicyclohexyl-[3,6-dimethoxy-2-(2,4,6-thisopropylphenyl)phenyl]phosphane (BrettPhos, 64.9 mg, 0.121 mmol) in anhydrous 1,4-dioxane (9 mL) was flushed with argon for 3 min. Tris(dibenzylideneacetone)dipalladium(0) (106 mg, 0.116 mmol) was added and the mixture was heated in a sealed flask to 70° C. for 2.5 hours. The reaction mixture was cooled to room temperature, diluted with EtOAc, filtered through kieselguhr and the filtrate was concentrated under reduced pressure to yield 1.5 g of a brown oil which was purified by flash chromatography (silica, gradient of 0.5 to 3% methanol in dichloromethane). 267 mg of a light-yellow oil were obtained (0.942 mmol), 37%). MS (ESI) m/z=284.2 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260441B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-596f38200ba849fc999a56d077cf684e |
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| Source note | uspto-grants-2016_02 |
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