HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104449Generated: October 29, 2026
Dimethylamine, hydrochloride → HCID 9808345, compound
https://huagongshe.com/reaction/2104449
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | HCID 68446914 | HCID 68446914 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 9808345 | HCID 9808345 | 118.7% |
Reaction Steps
Triethylamine (0.25 mL), dimethylamine hydrochloride (133 mg), 1-hydroxybenzotriazole monohydrate (53 mg) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (75 mg) were added to a chloroform suspension (10 mL) of the compound (168 mg) obtained in Example 56, and the mixture was stirred for 72 hours. The solvent was distilled away under reduced pressure. Water was added to the residue, and the mixture was extracted with chloroform. The resultant organic layer was washed with saturated brine and dried over magnesium sulfate anhydrate. The solvent was distilled away under reduced pressure, and the resultant residue was purified by silica gel column chromatography (methylene chloride:methanol=93:7). The thus-obtained colorless solids (135 mg) were suspended in ethanol (5 mL), and then 1N HCl in ethanol (0.5 mL) was added. The mixture was stirred for 2 hours, and the solvent was distilled away to give the title compound (112 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576135B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-1207299171af4db98205e85bc973c1de |
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| Source note | uspto-grants-2009_08 |
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