HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360905Generated: November 1, 2026
HCID 86623159, compound → HCID 11999019, compound
https://huagongshe.com/reaction/1360905
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86623159 | HCID 86623159 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 11999019 | HCID 11999019 | 43% |
Reaction Steps
N-(5-{2-bromo-5-[(3-hydroxypiperidin-1-yl)sulfonyl]-3-thienyl}-4-methyl-1,3-thiazol-2-yl)acetamide obtained in Step I as described above (54 mg; 0.112 mmol; 1 eq), is dissolved in dry TBF (5 ml) at −70° C. under an inert atmosphere. n-Butyllithium (0.15 ml; 1.6 M; 0.24 mmol; 2.20 eq) is added slowly and reaction stirred at −70° C. for 1 hour before being hydrolyzed with water (0.3 ml). Reaction is warmed up to room temperature before being concentrated to dryness. Residue is taken up with water (2 ml) and EtOAc (10 ml). The organic phases are decanted, dried over MgSO4, filtrated and evaporated. Title compound is purified by reverse preparative HPLC, affording expected Compound (48) as a white solid (20 mg; 43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879888B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-3ce66e6694f44c9aa4842dadb222c038 |
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| Source note | uspto-grants-2011_02 |
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