HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948432Generated: October 30, 2026
HCID 86623152, compound → HCID 11998796, compound
https://huagongshe.com/reaction/1948432
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86623152 | HCID 86623152 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11998796 | HCID 11998796 | 87% |
Reaction Steps
N-(5-{2-Bromo-5-[(2-dimethylamino-ethyl)-methyl-sulfamoyl]-thiophen-3-yl}-4-methyl-thiazol-2-yl)-acetamide obtained in Step I as described above (750 mg; 1.56 mmol; 1 eq), is dissolved in anhydrous THF (60 ml). The reaction mixture is cooled down to −70° C. and put under nitrogen. n-Butyllithium (6.2 ml; 1.6 M; 12.5 mmol; 8 eq) is added dropwise. The reaction is stirred 1 hour and is quenched with water. Solvents are evaporated and the resulting residue is dissolved in EtOAc, washed with water (2 times), brine and dried over MgSO4. After evaporation of the solvent, the resulting product is suspended in a mixture of ether-DCM and filtered, affording Compound (36) as a brown solid (582 mg; 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399497B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-1d9fe42154cb4aedb0c6dff751c27197 |
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| Source note | uspto-grants-2013_03 |
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