HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270102Generated: October 25, 2026
Ethyl Acetate → 4-[4-(2-fluoro-benzenesulfonyl)-2,2-dimethyl-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl]-piperazine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1270102
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 8-bromo-4-(2-fluorobenzenesulfonyl)-2,2-dimethyl-3,4-dihydro-2H-benzo[1,4]oxazine | HCID 22557282 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Binap, (A+-)- | HCID 634876 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-[4-(2-fluoro-benzenesulfonyl)-2,2-dimethyl-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl]-piperazine-1-carboxylic acid tert-butyl ester | HCID 58842135 | 82.7% |
Reaction Steps
A solution of 8-bromo-4-(2-fluoro-benzenesulfonyl)-2,2-dimethyl-3,4-dihydro-2H-benzo[1,4]oxazine (450 mg, 1.124 mmol) and 1-Boc-piperazine (209.4 mg, 1.124 mmol) in 5 mL of toluene was added to a warm, degassed mixture of Pd2(dba)3(Tris(dibenzylideneacetone)dipalladium(0), 20.59 mg, 0.022 mmol), BINAP (2,2′-bis(diphenylphosphino)-1,1′-binaphthyl, 35.0 mg, 0.056 mmol) and NaOt-Bu (151.26 mg, 1.57 mmol) in 5 ml of toluene. With stirring, the solution was heated at 90° C. for 2 hours, and then allowed to cool to room temperature. Ethyl acetate was added to the reaction which was then filtered through celite. The filtrate was washed with water (2×15 ml), brine (1×15 ml), and dried over MgSO4, after which the organic fraction was concentrated in vacuo. The resulting residue was purified by flash chromatography (15%–30% Ethyl acetate/Hexane) to give 470 mg (0.93 mmol) of 4-[4-(2-fluoro-benzenesulfonyl)-2,2-dimethyl-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl]-piperazine-1-carboxylic acid tert-butyl ester. MS: (M+H) 506.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07202241B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-ba0eb1bdddf044958b4c73be1e8da8ac |
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| Source note | uspto-grants-2007_04 |
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