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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13123Generated: October 25, 2026

Diisopropylamine → S-1-(4-Fluorophenyl)-1H-indazol-5-yl benzothioate

https://huagongshe.com/reaction/13123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant3,4,7,8-Tetramethyl-1,10-phenanthrolineHCID 74265—
Reactant1-(4-fluorophenyl)-5-iodo-1H-indazoleHCID 59251128—
ReactantHCID 178526132HCID 178526132—
CatalystHCID 178505377HCID 178505377—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductS-1-(4-Fluorophenyl)-1H-indazol-5-yl benzothioateHCID 5933984820%

Reaction Steps

To a solution of 1-(4-fluorophenyl)-5-iodo-1H-indazole (103e, 0.224 g, 0.66 mmol), thiobenzoic acid (0.093 ml, 0.79 mmol), 3,4,7,8-tetramethyl-1,10-phenantroline (0.031 g, 0.13 mmol) and N,N-diisopropylamine (0.220 ml, 1.32 mmol) in toluene (2.5 ml) was added copper(I) iodine (2.245 μl, 0.07 mmol). The resulting mixture was stirred at 110 C O/N. The reaction mixture was cooled to r.t. diluted with EtOAc and washed with water. The organic phase was the dried the solvent evaporated and then purified on HPLC. The relevant fractions were collected freezdried to give 45 mg of product (20% yield) which was analysed by LC/MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728030B2
Source datasetuspto-grants-2010_06
ORD IDord-5b1dc549e4134f18b2f42ea77cf3f868
Source noteuspto-grants-2010_06