HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-(Methylsulfanyl-pyrimidine-4-carbonyl)hexahydro-pyridazine-3-carboxylic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Methylsulfanyl-pyrimidine-4-carbonyl chloride | HCID 11542901 | — |
| Reactant | Methyl hexahydropyridazine-3-carboxylate | HCID 20596490 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Methylsulfanyl-pyrimidine-4-carbonyl)hexahydro-pyridazine-3-carboxylic acid methyl ester | HCID 23526870 | 36% |
Reaction Steps
To a solution of hexahydro-pyridazine-3-carboxylic acid methyl ester (1.5 g, 8.3 mmol) in CH2Cl2 (80 mL) is added 2-methylsulfanyl-pyrimidine-4-carbonyl chloride, 16, (1.41 g, 7.5 mmol) and triethylamine (1.2 mL, 8.3 mmol). The mixture is stirred at room temperature for 3 hours. The reaction solution is then diluted with1 N HCl (100 mL) and the organic phase is decanted. The aqueous phase is extracted with additional solvent and the organic layers are combined, dried, and concentrated in vacuo. The crude product is purified over silica(ethyl acetate/hexane 1:1) to afford 0.9 g (36% yield) of the desired product as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06821971B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-dc92d9e05a3844878c54af1fabfcebb6 |
| Source note | uspto-grants-2004_11 |