HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 4-(2,4-dicarboxyphenyl)-5-methyl-2-[N-(alpha-cyclopropylbenzyl)-N-propylamino]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-Bromo-1-(2,4-dibromophenyl)-1-propanone | HCID 18967754 | — |
| Reactant | N-(alpha-cyclopropylbenzyl)-N-propylthiourea | HCID 18967810 | — |
| Reactant | 4-(2,4-dibromophenyl)-5-methyl-2-[N-(alpha-cyclopropylbenzyl)-N-propylamino]thiazole | HCID 18967833 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | 4-(2,4-dicarboxyphenyl)-5-methyl-2-[N-(alpha-cyclopropylbenzyl)-N-propylamino]thiazole | HCID 18967803 | — |
Reaction Steps
5 ml of a 1.7M solution of tert-butyllithium in pentane are added, at -70° C., to 1.1 g of 4-(2,4-dibromophenyl)-5-methyl-2-[N-(α-cyclopropylbenzyl)-N-propylamino]thiazole (prepared from 2-bromo-1-(2,4-dibromophenyl)-1-propanone (Compound 14) and N-(α-cyclopropylbenzyl)-N-propylthiourea (Compound 65), according to the process described in Example 1, Step A), dissolved in 30 ml of anhydrous ethyl ether. The temperature is allowed to rise to -50° C. and the mixture is then subjected to the action of carbon dioxide, allowing the temperature to rise to 20° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05821255 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-79a105e8bb0e4a459e9296d641bfcd60 |
| Source note | uspto-grants-1998_10 |