HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 22011939, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4,5-Dichloro-6-ethylpyrimidine | HCID 11137668 | — |
| Reactant | HCID 22011938 | HCID 22011938 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22011939 | HCID 22011939 | — |
Reaction Steps
1.50 g (8.5 mmol) of 4,5-dichloro-6-ethylpyrimidine, 1.39 g (8.5 mmol) of 4-amino-2-phenyltetrahydrofuran and 2 ml (14 mmol) of triethylamine were heated for 12 hours at 85° C. After cooling, the mixture was diluted with water and extracted with ether, and the organic phase was washed with saturated NaCl solution. After the mixture had been dried and concentrated, the residue was purified by column chromatography using petroleum etherlethyl acetate (9:1, 8:2). This gave 1.63 g (63% of theory) of a colorless oil (diastereomers 1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06207668B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-d34792147bef4462a54114a73ac56575 |
| Source note | uspto-grants-2001_03 |