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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645150Generated: October 30, 2026

3-Bromo-5-(trifluoromethyl)benzenesulfonyl chloride → HCID 44611775, compound

https://huagongshe.com/reaction/1645150

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-5-(trifluoromethyl)benzenesulfonyl chlorideHCID 2778610—
ReactantHCID 59152881HCID 59152881—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
ProductHCID 44611775HCID 4461177573.5%

Reaction Steps

To a solution of ((R)-4-amino-4,5,6,7-tetrahydro-indazol-1-yl)-acetic acid ethyl ester (446 mg, 2.0 mmol) and 3-bromo-5-trifluoromethyl-benzenesulfonyl chloride (970 mg, 3.0 mmol) in tetrahydrofuran (5 mL) was added a solution of dimethyl-pyridin-4-yl-amine (489 mg, 4.0 mmol) in tetrahydrofuran (5 mL) dropwise. After being stirred at room temperature overnight, the mixture was concentrated. The residue was purified by column chromatography (gradient elution, 0-5% methanol in dichloromethane) to afford [(R)-4-(3-bromo-5-trifluoromethyl-benzenesulfonylamino)-4,5,6,7-tetrahydro-indazol-1-yl]-acetic acid ethyl ester (750 mg, 63.6%) as a white solid. MS calcd. for C18H19BrF3N3O4S 509, obsd. (ESI+) [(M+H)+] 510.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124641B2
Source datasetuspto-grants-2012_02
ORD IDord-cd3f8a3d03314bafbeb6023a3cb05601
Source noteuspto-grants-2012_02