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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (E)-3-(3-Acetoxy-4-methoxyphenyl)acrylic acid | HCID 14214114 | — |
| Reactant | 1-(3-methyl-3H-imidazol-4-ylmethyl)-1H-indol-7-ylamine | HCID 67337892 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (E)-3-(3-hydroxy-4-methoxy-phenyl)-N-[1-(3-methyl-3H-imidazol-4-ylmethyl)-1H-indol-7-yl]-acrylamide | HCID 67337739 | 33.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08470831B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-aef91be117ac428b89201c46e4fc16e8 |
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| Source note | uspto-grants-2013_06 |
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