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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391607Generated: November 2, 2026

5-Amino-2-methylbenzenesulfonamide → HCID 10218748, compound

https://huagongshe.com/reaction/1391607

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-2-methylbenzenesulfonamideHCID 235511—
ReactantHCID 59674158HCID 59674158—
ProductHCID 10218748HCID 1021874854.4%

Reaction Steps

The title compound was prepared following the procedure of example 5 using (4-tert-Butyl-phenyl)-{5-[(2-chloro-pyrimidin-4-yl)-methyl-amino]-1-methyl-1H-benzoimidazol-2-yl}-carbamic acid tert-butyl ester (104 mg, 0.20 mmol) and 5-amino-2-methyl-benzenesulfonamide (37 mg, 0.20 mmol) to give the desired product as a white solid (66 mg, 48%). 1H NMR (300 MHz, d6-DMSO+NaHCO3) δ 9.35 (s, 1H), 8.96 (s, 1H), 8.62 (s, 1H), 7.71-7.78 (m, 4H), 7.32-7.38 (M, 3H), 7.27 (s, 1H), 7.17-7.23 (M, 3H), 6.96 (d, J=8.4 Hz, 1H), 5.63 (d, J=6.0 Hz, 1H), 3.74 (s, 3H), 3.48 (s, 3H), 2.50 (s, 3H), 1.28 (s, 9H). MS (ESI) m/z=571 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07338959B2
Source datasetuspto-grants-2008_03
ORD IDord-6a16181959ce4d999aa67db9f8015369
Source noteuspto-grants-2008_03