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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1512167Generated: November 4, 2026

Ammonium Chloride → (E)-N-(3-amino-2'-trifluoromethyl-biphenyl-4-yl)-3-(tetrahydro-pyran-4-yl)-acrylamide

https://huagongshe.com/reaction/1512167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67528873HCID 67528873—
CatalystIronHCID 23925—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product(E)-N-(3-amino-2'-trifluoromethyl-biphenyl-4-yl)-3-(tetrahydro-pyran-4-yl)-acrylamideHCID 67527695—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of (E)-N-(3-nitro-2′-trifluoromethyl-biphenyl-4-yl)-3-(tetrahydro-pyran-4-yl)-acrylamide (82.0 mg, 0.195 mmol) in MeOH (5 mL) and water (5 mL) was treated with NH4Cl (104 mg, 1.95 mmol) and Fe powder (54.5 mg, 0.975 mmol) and heated to 50° C. for 1 h. The cooled mixture was treated with saturated aqueous NaHCO3 (30 mL) and extracted with EtOAc (2×30 mL). The combined organic layers were dried over MgSO4 and concentrated in vacuo to yield (E)-N-(3-amino-2′-trifluoromethyl-biphenyl-4-yl)-3-(tetrahydro-pyran-4-yl)-acrylamide as a colorless glassy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217060B2
Source datasetuspto-grants-2012_07
ORD IDord-7405234268964ebba2bcf4b2b1c61be1
Source noteuspto-grants-2012_07