Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | HCID 13255884 | HCID 13255884 | — |
| Product | HCID 20332980 | HCID 20332980 | — |
Reaction Steps
310 ml (0.226 mole) of a 33% ethanolic dimethylamine solution is added to a suspension of 45.0 g (0.11 mole) of 1-[2-(o-chlorobenzoyl)-4-chlorophenyl]-5-(chloromethyl)-1H-1,2,4-triazole-3-carboxylic acid (see DT-OS 2,159,527, page 32) and 0.5 g (0.0033 mole) of sodium iodide in 250 ml of methanol, and the mixture is stirred for 6 hours at room temperature. The clear reaction solution is concentrated in vacuo; the residue is dissolved in 200 ml of water, and 2 N hydrochloric acid solution is slowly added until the pH value of 5 is reached. After 16 hours' standing at 0°-5°, the precipitated aminic acid is filtered off and well washed with water and then with ether. Upon drying, there is obtained 1-[2-(o-chlorobenzoyl)-4-chlorophenyl]-5-[(dimethylamino)-methyl]-1H-1,2,4-triazole-3-carboxylic acid, m.p. 222°-225° with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04209516 |
|---|
| Source dataset | uspto-grants-1980_06 |
|---|
| ORD ID | ord-7db8ef4b99b6477bac369b22abe1ed07 |
|---|
| Source note | uspto-grants-1980_06 |
|---|