HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbonyl bromide → N-[4-(Isopropylformylamino)cyclohexyl]methylthiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbonyl bromide | HCID 79057 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | HCID 17946834 | HCID 17946834 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[4-(Isopropylformylamino)cyclohexyl]methylthiourea | HCID 22254060 | — |
Reaction Steps
A thiourea such as N-[4-(isopropylformylamino)cyclohexyl]-methylthiourea (0.029 mmol, 1 equivalent), a bromoketone (0.044 mmol, 1.5 equivalent) and 2 equivalents of diisopropylethyl amine in 10 ml of EtOH were heated at reflux temperature for 2 days. The reaction mixture was concentrated in vacuo and the crude product chromatographed (silica) to obtain the desired product. This procedure was used to prepare examples 101–102.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07189720B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-ee9773061a0943b58a1861525ed730a9 |
| Source note | uspto-grants-2007_03 |