HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852800Generated: October 26, 2026
1,2-Dibromoethane → HCID 178518178, compound
https://huagongshe.com/reaction/852800
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | HCID 178516948 | HCID 178516948 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178518178 | HCID 178518178 | — |
Reaction Steps
To a solution of 2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)thiazol-4(5H)-one (2.98 g, 14.2 mmol) in THF (15 ml) at −78° C. was added LDA (2.0 N, 28.4 ml). After 5 min, 1,2-dibromoethane (4.87 mL, 56.8 mmol) was added, and the reaction mixture was stirred for 3 h at −78° C. The resulting reaction mixture was poured into sat'd NaH2PO4 and extracted with EtOAc. The organic layer was dried over MgSO4, filtered and concentrated in vacuo. The crude residue was purified by flash chromatography (4:1; Hexane:EtOAc) to give the title compound as a white solid. MS (ES+): 317 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253196B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-57ae53f9ce1d44caa8c59ff210596670 |
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| Source note | uspto-grants-2007_08 |
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