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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591214Generated: November 1, 2026

Benzenesulfonyl chloride → HCID 67513798, compound

https://huagongshe.com/reaction/591214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
Reactant3-Iodo-5-(1-methyl-1H-pyrazol-4-YL)-1H-pyrrolo[2,3-B]pyridineHCID 66778502—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 67513798HCID 6751379890%

Reaction Steps

The 3-iodo-5-(1-methylpyrazol-4-yl)-7-azaindole prepared in accordance with WO 2008155000 (34 g) is suspended in 350 ml of dichloromethane, and 43.5 ml of triethylamine and 2.6 g of 4-(dimethylamino)pyridine are added. 17.5 ml of benzenesulfonyl chloride which has previously been diluted with 150 of dichloromethane are added to this mixture. After 2 h, the reaction is complete. The organic phase is extracted three times with water, and the organic phase is dried over sodium sulfate. After removal of the solvent, the residue is taken up in ethyl acetate, the precipitate is filtered off, rinsed with ethyl acetate, and the product is dried in air to give 44 g (90%) of beige crystals; (Rt: 2.467 min; M+H+: 464.9).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238651B2
Source datasetuspto-grants-2016_01
ORD IDord-861a55ff978e4b6481f343007e09dea7
Source noteuspto-grants-2016_01