Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645162Generated: October 30, 2026

Ammonium Chloride → (R)-[4-(3-isopropenyl-5-trifluoromethyl-benzenesulfonylamino)-4,5,6,7-tetrahydro-indazol-1-yl]-acetic acid ethyl ester

https://huagongshe.com/reaction/1645162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolaneHCID 10997426—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 44611775HCID 44611775—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product(R)-[4-(3-isopropenyl-5-trifluoromethyl-benzenesulfonylamino)-4,5,6,7-tetrahydro-indazol-1-yl]-acetic acid ethyl esterHCID 5915288936.8%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a solution of [(R)-4-(3-bromo-5-trifluoromethyl-benzenesulfonylamino)-4,5,6,7-tetrahydro-indazol-1-yl]-acetic acid ethyl ester (Example 1-1, 100 mg, 0.196 mmol) in N,N-dimethylformamide (2 mL) in a microwave vial (5 mL), tetrakis(triphenylphosphine)palladium(0) (22 mg, 0.19 mmol), potassium tert-butoxide (45 mg, 0.4 mmol) and isopropenyl boronic acid pinacol ester (55 μl, 0.294 mmol) were added. After being heated in a microwave oven (130° C., 15 min.), the mixture was poured into aq. ammonium chloride (10 mL) and extracted with dichloromethane (20 mL×3). The combined organic layers were washed with water (10 mL×3) and brine (20 mL), dried over sodium sulfate and concentrated in vacuo. The residue was purified by column chromatography (gradient elution, 0-5% methanol in dichloromethane) to afford [(R)-4-(3-isopropenyl-5-trifluoromethyl-benzene-sulfonylamino)-4,5,6,7-tetrahydro-indazol-1-yl]-acetic acid ethyl ester (34 mg, 36.8%) as a white solid, MS calcd. for C21H24F3N3O4S 471, obsd. (ESI+) [(M+H)+] 472.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124641B2
Source datasetuspto-grants-2012_02
ORD IDord-f2dcc566ef784746a174ac625fb306a0
Source noteuspto-grants-2012_02