HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(6-Phenylacetylenyl-2-benzothiazolyl)-3-ethylurea → 1-(6-(2(Z)-Phenylvinyl)-2-benzothiazolyl)-3-ethylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(6-Phenylacetylenyl-2-benzothiazolyl)-3-ethylurea | HCID 21985545 | — |
| Catalyst | Lindlars catalyst | HCID 131709914 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(6-(2(Z)-Phenylvinyl)-2-benzothiazolyl)-3-ethylurea | HCID 86588973 | 41% |
Reaction Steps
A suspension of 1-(6-phenylacetylenyl-2-benzothiazolyl)-3-ethylurea (0.032 g, 83% purity by weight, 0.083 mmol) and Lindlar catalyst (0.030 g, 5% weight purity, 0.012 mmol, 0.15 eq) in 2 mL ethanol was purged with nitrogen gas, followed by bubbling of hydrogen gas. It was stirred under hydrogen atmosphere for about 36 hours. The mixture was taken up in 10 mL MeOH, filtered, concentrated, and purified by preparative TLC to give 0.011 g (41%) of the desired compound. LC/MS 324 (M+1); LC retention time 2.84 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091227B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-b034843c1eae49b58ee346d1b1960c87 |
| Source note | uspto-grants-2006_08 |