HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorobenzamide → HCID 66762338, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorobenzamide | HCID 71572 | — |
| Reactant | 5-(trifluoromethyl)pyridine-2-carbothioamide | HCID 2777773 | — |
| Reactant | Methyl 4-bromo-3-oxopentanoate | HCID 9815681 | — |
| Reactant | HCID 22563305 | HCID 22563305 | — |
| Product | HCID 66762338 | HCID 66762338 | — |
Reaction Steps
The title compound was prepared in analogy to example 31 (steps A] and C] as outlined for example 31 and step B] according to example 33) starting from 2-[5-methyl-2-(5-trifluoromethyl-pyridin-2-yl)-thiazol-4-yl]-ethanol. This starting material could be prepared from 5-trifluoromethyl-2-pyridinecarbothioamide [CAS 175277-51-7, commercially available] and methyl-4-bromo-3-oxopentanoate with 4-fluoro-benzamide as described in Collins, J. L. et al. J. Med. Chem. 1998, 41, 5037-5054. The compound was obtained as a yellow gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07314884B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-23eb5a64c3d84fe7b3b45c74e474bfe6 |
| Source note | uspto-grants-2008_01 |