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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17128Generated: October 29, 2026

Ammonium Chloride → n-[4-(4,7-Diamino-2-methylthieno[3,2-c]pyridin-3-yl)phenyl]-n'-(3-methylphenyl)urea

https://huagongshe.com/reaction/17128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactantn-[4-(4-Amino-2-methyl-7-nitrothieno[3,2-c]pyridin-3-yl)phenyl]-n'-(3-methylphenyl)ureaHCID 18450935—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Productn-[4-(4,7-Diamino-2-methylthieno[3,2-c]pyridin-3-yl)phenyl]-n'-(3-methylphenyl)ureaHCID 1845093336.8%

Reaction Steps

A suspension of Example 66E (0.44 g, 1.01 mmol), NH4Cl (0.054 g, 1.01 mmol), and iron powder (0.45 g, 8.1 mmol) in ethanol (16 mL) and water (4 mL) was heated at 80° C. for 3 hours, cooled to room temperature, and filtered through diatomaceous earth (Celite®). The pad was washed with ethyl acetate and ethanol and the filtrate was extracted three times with ethyl acetate. The combined extracts were washed with brine, dried (Na2SO4), filtered, and concentrated. The residue was purified by flash column chromatography on silica gel with 5% methanol/dichloromethane to provide 0.15 g of the desired product. 1H NMR (300 MHz, DMSO-d6) δ 2.27 (s, 3H), 2.29 (s, 3H), 4.48 (s, 2H), 4.59 (s, 2H), 6.80 (d, J=7.46 Hz, 1H), 7.17 (t, J=7.80 Hz, 1H), 7.25-7.29 (m, 3H), 7.30 (s, 1H), 7.31 (s, 1H), 7.60 (d, J=8.81 Hz, 2H), 8.67 (s, 1H), 8.86 (s, 1H); MS (ESI(+)) m/e 404 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737160B2
Source datasetuspto-grants-2010_06
ORD IDord-59eb91be7fc548d38601a3465f5fa4e5
Source noteuspto-grants-2010_06