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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391572Generated: November 2, 2026

Benzenesulfonamide, 3-amino- → 3-(4-{[2-(3-Fluoro-benzylamino)-1-methyl-1H-benzoimidazol-5-yl]-methyl-amino}-pyrimidin-2-ylamino)-benzenesulfonamide hydrochloride

https://huagongshe.com/reaction/1391572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonamide, 3-amino-HCID 7377—
ReactantHCID 59674229HCID 59674229—
Product3-(4-{[2-(3-Fluoro-benzylamino)-1-methyl-1H-benzoimidazol-5-yl]-methyl-amino}-pyrimidin-2-ylamino)-benzenesulfonamide hydrochlorideHCID 10239887—

Reaction Steps

The title compound was prepared following the procedure of example one with N5-(2-chloro-pyrimidin-4-yl)-N2-(3-fluoro-benzyl)-1,N5-dimethyl-1H-benzoimidazole-2,5-diamine (99 mg, 0.25 mmol) and 3-amino-benzenesulfonamide (43 mg, 0.25 mmol) as a white solid (62 mg, 44%). 1H NMR (300 MHz, d6-DMSO+NaHCO3) δ 9.70 (s, 2H), 8.53 (s, 1H), 7.83 (d, J=6.0 Hz, 1H), 7.74 (d, J=6.6 Hz, 1H), 7.26-7.50 (M, 8H), 7.10 (m, 2H), 5.69 (d, J=6.0 Hz, 1H), 4.70 (d, J=5.1 Hz, 2H), 3.67 (s, 3H), 3.46 (s, 3H). MS (ESI) m/z=533 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07338959B2
Source datasetuspto-grants-2008_03
ORD IDord-ddc7e410ecd34279aff644a5a0bd650b
Source noteuspto-grants-2008_03