Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260385Generated: October 31, 2026

Thionyl Chloride → (E)-3-(3-hydroxy-4-methoxy-phenyl)-N-[1-(3-methyl-3H-imidazol-4-ylmethyl)-1H-indol-7-yl]-acrylamide

https://huagongshe.com/reaction/1260385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(E)-3-(3-Acetoxy-4-methoxyphenyl)acrylic acidHCID 14214114—
Reactant1-(3-methyl-3H-imidazol-4-ylmethyl)-1H-indol-7-ylamineHCID 67337892—
SolventTetrahydrofuranHCID 8028—
Product(E)-3-(3-hydroxy-4-methoxy-phenyl)-N-[1-(3-methyl-3H-imidazol-4-ylmethyl)-1H-indol-7-yl]-acrylamideHCID 6733773933.1%

Reaction Steps

(E)-3-(3-Acetoxy-4-methoxyphenyl)acrylic acid (0.099 g, 0.420 mmol) was suspended in dry THF (8 ml). SOCl2 (0.037 ml, 0.504 mmol) was added and the mixture was stirred at RT for 1 h. The solvent was evaporated to dryness and the residue was dissolved in dry THF (8.00 ml). TEA (0.059 ml, 0.420 mmol) and 1-(3-methyl-3H-imidazol-4-ylmethyl)-1H-indol-7-ylamine (0.095 g, 0.420 mmol) were added. The mixture was stirred at RT for 18 hrs, heated at reflux for hrs and then at RT for 48 hrs. The solvent was removed in vacuo and the residue was partitioned between EtOAc (10 ml) and H2O (2×10 ml). Organic phase was dried over sodium sulphate and concentrated to dryness. The crude was charged onto a SCX cartridge and eluted firstly with MeOH and then with NH3/MeOH. The title (E)-3-(3-hydroxy-4-methoxy-phenyl)-N-[1-(3-methyl-3H-imidazol-4-ylmethyl)-1H-indol-7-yl]-acrylamide (56 mg) was obtained after column chromatography (eluent: DCM 100% to DCM/MeOH 98:2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470831B2
Source datasetuspto-grants-2013_06
ORD IDord-aef91be117ac428b89201c46e4fc16e8
Source noteuspto-grants-2013_06