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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879380Generated: October 27, 2026

Lithium Chloride → (S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-2-(1,2-dimethyl-3-oxo-2,3-dihydro-1H-indazol-6-yl)-5-methylbenzo[d]thiazol-6-yl)acetate

https://huagongshe.com/reaction/879380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium ChlorideHCID 433294—
Reactant(S)-ethyl 2-(2-bromo-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyacetateHCID 86700141—
Reactant1,2-dimethyl-6-(tributylstannyl)-1H-indazol-3(2H)-oneHCID 86700175—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product(S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-2-(1,2-dimethyl-3-oxo-2,3-dihydro-1H-indazol-6-yl)-5-methylbenzo[d]thiazol-6-yl)acetateHCID 86700190—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of (S)-ethyl 2-(2-bromo-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyacetate (30.0 mg, 0.060 mmol) and 1,2-dimethyl-6-(tributylstannyl)-1H-indazol-3(2H)-one (32.5 mg, 0.072 mmol) in dioxane (0.7 mL) was added Pd(PPh3)4 (7.0 mg, 0.006 mmol), CuI (4.0 mg, 0.018 mmol) and LiCl (8.0 mg, 0.182 mmol). The reaction was degassed for 5 minutes with N2 and then heated at 100° C. for 7 h. After cooling, the reaction mixture was diluted with EtOAc, extracted with H2O, brine, dried over Na2SO4, filtered and concentrated and purified by flash column chromatography (silica gel, 0 to 100% ethyl acetate/hexanes) to give the desired product. LCMS-ESI+ (m/z): [M+H]+ calcd for C31H33ClN3O4S: 578.2; found: 578.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987250B2
Source datasetuspto-grants-2015_03
ORD IDord-3bcacc4167bd4dbe8f7b60bafc1b4e96
Source noteuspto-grants-2015_03