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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391562Generated: November 4, 2026

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

https://huagongshe.com/reaction/1391562

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-2-methylbenzenesulfonamideHCID 235511—
ReactantN5-(2-chloro-pyrimidin-4-yl)-N2-(4-fluoro-benzyl)-1,N5-dimethyl-1H-benzoimidazole-2,5-diamineHCID 59674181—
Product5-(4-{[2-(4-Fluoro-benzylamino)-1-methyl-1H-benzoimidazol-5-yl]-methyl-amino}-pyrimidin-2-ylamino)-2-methyl-benzenesulfonamide hydrochlorideHCID 10239978—

Reaction Steps

The title compound was prepared following the procedure of example one with N5-(2-chloro-pyrimidin-4-yl)-N2-(4-fluoro-benzyl)-1,N5-dimethyl-1H-benzoimidazole-2,5-diamine (99 mg, 0.25 mmol) and 5-amino-2-methyl-benzenesulfonamide (47 mg, 0.25 mmol) as a white solid (69 mg, 48%). 1H NMR (300 MHz, d6-DMSO+NaHCO3) δ10.28 (br s, 1H), 9.61 (br s, 1H), 8.45 (s, 1H), 7.86 (d, J=2.1 Hz, 1H), 7.63 (m, 1H), 7.52-7.59 (m, 3H), 7.37 (s, 1H), 7.31 (s, 2H), 7.13-7.26 (m, 4H), 5.74 (d, J=4.5 Hz, 1H), 4.73 (d, J=4.5 Hz, 2H), 3.71 (s, 3H), 3.48 (s, 3H), 2.50 (s, 3H). MS (ESI) m/z=547 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07338959B2
Source datasetuspto-grants-2008_03
ORD IDord-054da39c55c242debaabc1e124f5ee82
Source noteuspto-grants-2008_03