HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(2-bromoacetyl)benzoic Acid → HCID 18186612, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(2-bromoacetyl)benzoic Acid | HCID 2756836 | — |
| Reactant | ethyl 4-(carbamothioylamino)piperidine-1-carboxylate | HCID 11535967 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18186612 | HCID 18186612 | 70,161.203% |
Reaction Steps
A solution of ethyl 4-thioureidopiperidine-1-carboxylate (3.8 g, 0.0164 mol.) and 4-(2-bromoacetyl)benzoic acid (4 g, 0.0164 mmol) in THF (100 mL) was heated at 70° C. for 2 hours, cooled to room temperature and then diluted with diethyl ether. A resulting solid was collected by filtration and washed with diethyl ether to provide 4-[2-(1-ethoxycarbonylpiperidin-4-ylamino)thiazol-4-yl]benzoic acid (4.32 g, 70% yield) as an off white solid. HNMR (dmso-d6): 7.93 (4H, m), 7.27 (1H, s), 4.05 (2H, q), 3.82 (3H, m), 3.04 (2H, m), 2.02 (2H, m), 1.41 (2H, m), 1.18 (3H, t). LC/MS: M+1: 376.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06593327B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-e409ceacdd874eb8bb52f066e5f00c24 |
| Source note | uspto-grants-2003_07 |