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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110161Generated: October 31, 2026

Acetonitrile → HCID 131727400, compound

https://huagongshe.com/reaction/2110161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactantmethyl 4-(chlorosulfonyl)-2,3-dihydro-1H-indene-2-carboxylateHCID 46835233—
ReactantHCID 68959603HCID 68959603—
SolventWaterHCID 962—
ProductHCID 131727400HCID 131727400—

Reaction Conditions

Temperature55 °C

Reaction Steps

4-Chlorosulfonyl-indan-2(R,S)-carboxylic acid methyl ester (225 mg, 0.82 mmol) was added to a mixture of 1-(3-bromo-4-chlorophenyl)-cis-3,5-dimethylpiperazine (569 mg, 1.87 mmol), potassium carbonate (500 mg, 3.6 mmol), and acetonitrile (8 mL) at rt under nitrogen, and the reaction was heated at 55° C. for 3 h. After allowing the reaction to cool to rt, it was poured into water (40 mL) and extracted with dichloromethane (40 mL×2). The combined organic extracts were dried, filtered, concentrated, and purified by silica gel chromatography (9:1→3:1; hexanes:ethyl acetate) to give methyl 4-(4-(3-bromo-4-chlorophenyl)-cis-2,6-dimethylpiperazin-1-ylsulfonyl)-2,3-dihydro-1H-indene-2(R,S)-carboxylate: MS (ESI): 541.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517884B2
Source datasetuspto-grants-2009_04
ORD IDord-79da05b2dd8c469e8cf56ca52a6b29be
Source noteuspto-grants-2009_04