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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184539Generated: October 29, 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/1184539

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 5 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 numberUS08669261B2
Source datasetuspto-grants-2014_03
ORD IDord-a0a195db1e7b4623ae0a7378ca62b5c0
Source noteuspto-grants-2014_03