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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766276Generated: November 1, 2026

Benzenesulfonyl chloride → HCID 86592477, compound

https://huagongshe.com/reaction/1766276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 17980126HCID 17980126—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86592477HCID 86592477—

Reaction Steps

By a method similar to Example 31, using 9-(1-methylpiperidin-4-yl)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-7-ol (135 mg, 0.5 mmol), NaOH (3.25 mL, 0.65 mmol, 0.2 N), benzenesulfonyl chloride (99 mg, 0.564 mmol), and THF (1.5 mL) gave a crude residue which was purified by PCTLC (silica gel GF rotor; 95:5 CHCl3:2M NH3 in MeOH) and the hydrochloride was formed in EtOAc affording 196 mg (88%) of the title compound as an off-white powder: mp=202-204° C.; MS (ES+): m/e 411.0 (M+1); Calculated for C23H26N2O3S.HCl: C, 61.80; H, 6.09; N, 6.27. Found: C, 61.49; H, 6.10; N, 6.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230011B2
Source datasetuspto-grants-2007_06
ORD IDord-fc91c8e1b6fb4fd3aca505282b20ba2b
Source noteuspto-grants-2007_06