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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391592Generated: November 3, 2026

1-(4-Aminophenyl)methanesulfonamide → HCID 10240062, compound

https://huagongshe.com/reaction/1391592

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Aminophenyl)methanesulfonamideHCID 10821407—
ReactantHCID 59674100HCID 59674100—
ProductHCID 10240062HCID 10240062—

Reaction Steps

The title compound was prepared following the procedure of example one with N2-(4-Chloro-benzyl)-N5-(2-chloro-pyrimidin-4-yl)-1,N5-dimethyl-1H-benzoimidazole-2,5-diamine (103 mg, 0.25 mmol) and (4-amino-phenyl)-methanesulfonamide (46 mg, 0.25 mmol) as a white solid (90 mg, 60%). 1H NMR (300 MHz, d6-DMSO+NaHCO3) δ 9.31 (s, 1H), 8.05 (br s, 1H), 7.72-7.80 (m, 3H), 7.46 (d, J=8.4 Hz, 2H), 7.38 (d, J=8.4 Hz, 2H), 7.32 (d, J=8.4 Hz, 1H), 7.20 (d, J=8.4 Hz, 2H), 7.14 (s, 1H), 6.93 (d, J=8.4 Hz, 1H), 6.78 (s, 2H), 5.66 (d, J=6.0H, 1H), 4.62 (d, J=5.4 Hz, 2H), 4.17 (s, 2H), 3.63 (s, 3H), 3.44 (s, 3H). MS (ESI) m/z=563 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07338959B2
Source datasetuspto-grants-2008_03
ORD IDord-dc999a90d3bc4906a492eec5a1d46267
Source noteuspto-grants-2008_03