HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethyl bromide → HCID 178496612, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | HCID 178460750 | HCID 178460750 | — |
| Reactant | HCID 178496609 | HCID 178496609 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178496612 | HCID 178496612 | — |
Reaction Steps
The compound was prepared following an analogous procedure to the one described for the synthesis of 2-methyl-2-{2-[3-(trans-4-methyl-cyclohexyl)-3-phenethyl-ureido]-thiazol-5-ylsulfanyl}-propionic acid using trans-4-methoxy-cyclohexylamine (prepared as described in J. Med. Chem. 1977, 20, 279-290), 2-phenylethylbromide and 2-aminothiazol-5-ylsulfanyl)acetic acid ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08362049B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-40fa0ec531ca47b09744871652b7c100 |
| Source note | uspto-grants-2013_01 |