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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729729Generated: November 1, 2026

Water → HCID 86594315, compound

https://huagongshe.com/reaction/729729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 10383831HCID 10383831—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86594315HCID 86594315—

Reaction Steps

A stirred suspension of (E)-2-(4-nitrophenyl)-3-(tetrahydropyran-4-yl)-N-thiazol-2-ylacrylamide (EXAMPLE 81, 1.54 g, 4.0 mmol) in EtOH (54 mL) and THF (31 mL) was treated with H2O (13 mL), saturated aqueous NH4Cl (13 mL), and Fe powder (1.49 g, 26.7 mmol). After 4.5 h at 20° C., the reaction mixture was filtered through Celite, washing with CH2Cl2. The combined filtrates were concentrated and the residue was dissolved in CH2Cl2. The CH2Cl2 solution was washed with H2O and dried (MgSO4). Filtration, solvent evaporation, and column chromatography (EtOAc-MeOH, 19:1) gave (E)-2-(4-aminophenyl)-3-(tetrahydropyran-4-yl)-N-thiazol-2-ylacrylamide; m/z (ES+)=330.1 [M+H]+. A stirred solution of this compound (104 mg, 291 μmol) in anhydrous CH2Cl2 (4 mL) was treated with MeSO2Cl (90 μL, 1165 μmol) and pyridine (94 μL, 1165 μmol). After 16 h, the mixture was diluted with CH2Cl2 (25 mL), before being extracted twice with 2M NaOH. The combined aqueous extracts were washed with Et2O, before being acidified with 12M HCl to pH 1 and extracted twice with CH2Cl2. The combined organic extracts were washed with brine and dried (MgSO4). Filtration and solvent evaporation afforded the title compound: RTB=1.26 min; m/z (ES+)=408.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582632B2
Source datasetuspto-grants-2009_09
ORD IDord-f03f6a0ee3a746d0a746f97b5f8e439a
Source noteuspto-grants-2009_09