HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641694Generated: November 2, 2026
Dimethylamine, hydrochloride → HCID 57736440, compound
https://huagongshe.com/reaction/1641694
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 57736501 | HCID 57736501 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57736440 | HCID 57736440 | 99% |
Reaction Steps
To a solution of 5-[(2,5-difluorophenyl)[[6-(trifluoromethyl)pyridin-3-yl]thio]methyl]-4-methylpyridine-2-carboxylic acid (352 mg, 0.80 mmol) in methylene chloride (10 ml), dimethylamine hydrochloride (73 mg, 0.88 mmol), 1-hydroxybenzotriazole (119 mg, 0.88 mmol) 4-methylmorpholine (0.194 ml, 1.76 mmol), and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (169 mg, 0.88 mmol) were added at room temperature. After stirring for 13 hours at room temperature, the reaction mixture was washed with 0.5 N hydrochloric acid. The organic layer was dried over anhydrous sodium sulfate and filtered, then the filtrate was concentrated under reduced pressure, and the resulting residue was subjected to flash silica gel chromatography. The fraction obtained from an elution with hexane:ethyl acetate=1:1 was concentrated under reduced pressure to obtain the title compound (370 mg, 0.79 mmol, 99%) as a colorless oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08114886B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-bebe1333916f4451bb33a69dce99246b |
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| Source note | uspto-grants-2012_02 |
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