HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856505Generated: November 2, 2026
Dimethylformamide → HCID 69521907, compound
https://huagongshe.com/reaction/856505
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 7-[4-(2-Butoxyethoxy)phenyl]-1-isobutyl-2,3-dihydro-1-benzazepine-4-carboxylic acid | HCID 22328905 | — |
| Reactant | HCID 69521807 | HCID 69521807 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 69521907 | HCID 69521907 | 13.7% |
Reaction Steps
7-[4-(2-butoxyethoxy)phenyl]-1-isobutyl-2,3-dihydro-1-benzazepine-4-carboxylic acid (0.80 g) was dissolved in THF (16 ml), DMF (2 droplets) was added to the mixture, thionyl chloride (0.20 ml) was added to the mixture, and the solution was stirred at room temperature for 1 hour. The solution was added dropwise to a solution of 4-[(3-pyridazinylmethyl)sulfanyl]aniline (0.44 g) and triethylamine (2.55 ml) in THF (13.2 ml) under ice-cooling and the mixture was stirred for 2 hours at room temperature. The reaction solution was added to water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was removed under reduced pressure, and the obtained residue was purified with silica gel column chromatography, to give 7-[4-(2-butoxyethoxy)phenyl]-1-isobutyl-N-[4-[(3-pyridazinylmethyl)sulfanyl]phenyl]-2,3-dihydro-1-benzazepine-4-carboxamide (Compound 258) (0.16 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07262185B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-dcba192a247c4c46a1cd17bc7abfc315 |
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| Source note | uspto-grants-2007_08 |
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