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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360905Generated: November 1, 2026

HCID 86623159, compound → HCID 11999019, compound

https://huagongshe.com/reaction/1360905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86623159HCID 86623159—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
ProductHCID 11999019HCID 1199901943%

Reaction Conditions

Temperature-70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879888B2
Source datasetuspto-grants-2011_02
ORD IDord-3ce66e6694f44c9aa4842dadb222c038
Source noteuspto-grants-2011_02