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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391600Generated: November 2, 2026

4-[(methylsulfonyl)methyl]aniline(SALTDATA: FREE) → n5-[2-(4-Methanesulfonylmethyl-phenylamino)-pyrimidin-4-yl]-1,n5-dimethyl-n2-(4-methyl-benzyl)-1h-benzoimidazole-2,5-diamine hydrochloride

https://huagongshe.com/reaction/1391600

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(methylsulfonyl)methyl]aniline(SALTDATA: FREE)HCID 12843964—
ReactantHCID 59674205HCID 59674205—
Productn5-[2-(4-Methanesulfonylmethyl-phenylamino)-pyrimidin-4-yl]-1,n5-dimethyl-n2-(4-methyl-benzyl)-1h-benzoimidazole-2,5-diamine hydrochlorideHCID 10312120—

Reaction Steps

The title compound was prepared following the procedure of example one with N5-(2-Chloro-pyrimidin-4-yl)-1,N5-dimethyl-N2-(4-methyl-benzyl)-1H-benzoimidazole-2,5-diamine (98 mg, 0.25 mmol) and 4-[(methylsulfonyl)methyl]aniline (46 mg, 0.25 mmol) as a white solid (141 mg, 97%). 1H NMR (300 MHz, d6-DMSO+NaHCO3) δ 9.21 (s, 1H), 7.76-7.79 (M, 3H), 7.50 (br s, 1H), 7.22-7.30 (m, 5H), 7.09-7.14 (M, 3H), 6.86 (d, J=8.4 Hz, 1H), 5.64 (d, J=6.0 Hz, 1H), 4.55 (d, J=5.4 Hz, 2H), 4.34 (s, 2H), 3.58 (s, 3H), 3.43 (s, 3H), 2.85 (s, 3H), 2.26 (s, 3H). MS (ESI) m/z=542 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07338959B2
Source datasetuspto-grants-2008_03
ORD IDord-2475a70ff78c4e638f924400f1c8d2d1
Source noteuspto-grants-2008_03