HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 20267949, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Chloropyrimidin-2-ol hydrochloride | HCID 12648523 | — |
| Reactant | 5-[(Chloromethoxy)methyl]-4-methyl-2-(methylsulfanyl)pyrimidine | HCID 20267940 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20267949 | HCID 20267949 | — |
Reaction Steps
2-Methylthio-4-methyl-5-(chloromethyloxymethyl)pyrimidine (see Preparation 11) (2.7 mmol) in dichloromethane (5 ml) was added dropwise with stirring at room temperature to a solution of 5-chloropyrimidin-2-one hydrochloride (2.7 mmol) and triethylamine in dichloromethane (0.76 ml). The mixture was stirred for 24 hours at room temperature before the solvent was distilled off. The residue was triturated with water, extracted into chloroform and the dried (MgSO4) solution evaporated. yield 0.55 g (65%). 1H NMR (CDCl3): δ2.42 (4-Me), 2.55 (SMe), 4.65 (CH2Pyr), 5.32 (CH2O), 7.80 and 8.42 (H-4, H-6, J 3 Hz), 8.20 (H-6').
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04539324 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-7f9e2a72fd784b12b8c6742cf18ca2ba |
| Source note | uspto-grants-1985_09 |