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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086007Generated: October 30, 2026

P-Toluenesulfonamide → HCID 10270136, compound

https://huagongshe.com/reaction/2086007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-ToluenesulfonamideHCID 6269—
Reactant6(5h)-Phenanthridinone, 2-amino-HCID 270668—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 10270136HCID 1027013693%

Reaction Steps

Prepared from 2-amino-6(5H)-phenanthridinone 3 and 4-methyl benzenesulfonamide according to General Procedure A. P-dioxane was used as solvent and the reaction was run at 40° C. for 30 hours. Purification of compound by crystallization in dioxane gave a brown solid (93% yield). mp 199-203° C. 1H-NMR (400 MHz, DMSO-d6), 10.20 (s, 1H), 8.30 (d, J=8.0 Hz, 1H), 8.15 (d, J=8.1 Hz, 1H), 7.95 (s, 1H), 7.88 (t, J=7.6, 1H), 7.65 (m, 3H), 7.33 (d, J=8.2 Hz, 2H), 7.19 (m, 2H). Anal. (C20H16N2O3S), C H N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06723733B2
Source datasetuspto-grants-2004_04
ORD IDord-762ed160bbb541b29ddc2b9c4bedecfd
Source noteuspto-grants-2004_04