HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 1-Pyrimidin-2-yl-piperidine-4-carboxylic acid N'-(3-methyl-butyryl)-hydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-(Pyrimidin-2-yl)piperidine-4-carboxylic acid | HCID 2767267 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Pyrimidin-2-yl-piperidine-4-carboxylic acid N'-(3-methyl-butyryl)-hydrazide | HCID 23544067 | 46.4% |
Reaction Steps
The residue was added to a mixture of 1-pyrimidin-2-yl-piperidine-4-carboxylic acid (6.6 g, 31.7 mmol) (see reference U.S. Pat. No. 4,826,843), 1-hydroxybenzotriazole hydrate (4.28 g, 31.7 mmol) and 1-(3-dimethylaminopropyl-3-ethylcarbodiimide hydrochloride (6.09 g, 31.7 mmol) in dichloromethane (50 ml). Diisopropylethylamine (17 ml, 95 mmol) was added and the mixture was stirred for 3 days. The solvent was evaporated and the residue was triturated with water and then with diethyl ether to give the title compound as a white solid (4.49 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07084145B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-4c0cc20436e440c9a6f5ae1c9ddc1270 |
| Source note | uspto-grants-2006_08 |