HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16717Generated: October 26, 2026
1,2-Ethanediamine, N1,N1,N2-trimethyl- → HCID 178501159, compound
https://huagongshe.com/reaction/16717
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Ethanediamine, N1,N1,N2-trimethyl- | HCID 67338 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 178501163 | HCID 178501163 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178501159 | HCID 178501159 | 93.3% |
Reaction Steps
Trans-4-(methoxycarbonyl)cyclohexanecarboxylic acid (8.84 g) obtained in Reference Example 1(2) is dissolved in chloroform (100 ml), and thereto are added 1-hydroxybenzotriazole (7.14 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (10.00 g) and N,N,N′-trimethylethylenediamine (5.33 g) under ice-cooling. The mixture is then stirred at room temperature for 4 hours. Saturated aqueous sodium hydrogen carbonate solution is poured to the reaction solution and the mixture is extracted with chloroform. The organic layer is washed with saturated brine and dried over sodium sulfate. The solvent is concentrated under reduced pressure. The resulting residue is purified by silica gel column chromatography (eluent: chloroform/methanol/28% ammonia water=200/10/1) to give methyl trans-4-{[[2-(dimethylamino)ethyl](methyl)amino]carbonyl}-cyclohexanecarboxylate (11.98 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07737161B2 |
|---|
| Source dataset | uspto-grants-2010_06 |
|---|
| ORD ID | ord-8b58af24ecdb470eb2de945d1ee82651 |
|---|
| Source note | uspto-grants-2010_06 |
|---|