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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391568Generated: November 4, 2026

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

https://huagongshe.com/reaction/1391568

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(methylsulfonyl)methyl]aniline(SALTDATA: FREE)HCID 12843964—
ReactantHCID 59674096HCID 59674096—
Productn5-[2-(4-Methanesulfonylmethyl-phenylamino)-pyrimidin-4-yl]-n2-(4-methoxy-benzyl)-1,n5-dimethyl-1h-benzoimidazole-2,5-diamine hydrochlorideHCID 131726797—

Reaction Steps

The title compound was prepared following the procedure of example two with N5-(2-chloro-pyrimidin-4-yl)-N2-(4-methoxy-benzyl)-1,N5-dimethyl-1H-benzoimidazole-2,5-diamine (82 mg, 0.20 mmol) and 4-[(methylsulfonyl)methyl]aniline (37 mg, 0.20 mmol) as a white solid (86 mg, 72%). 1H NMR (300 MHz, d6-DMSO) δ 9.21 (s, 1H), 7.76-7.81 (m, 3H), 7.29-7.34 (m, 3H), 7.21-7.25 (m, 3H), 7.09 (d, J=1.8 Hz, 1H), 6.82-6.90 (M, 3H), 5.64 (d, J=6.0 Hz, 1H), 4.52 (d, J=5.7 Hz, 2H), 4.35 (s, 2H), 3.72 (s, 3H), 3.56 (s, 3H), 3.43 (s, 3H), 2.85 (s, 3H). MS (ESI) m/z=558 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07338959B2
Source datasetuspto-grants-2008_03
ORD IDord-f68a2ce7e6e642429560b4e74c343e02
Source noteuspto-grants-2008_03