HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → 1-Cyclohex-3-enyl-1-cyclohexyl-3-thiazol-2-yl-urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Bis-(1H-imidazol-2-YL)-methanone | HCID 5250894 | — |
| Reactant | Cyclohex-3-en-1-amine | HCID 13040867 | — |
| Product | 1-Cyclohex-3-enyl-1-cyclohexyl-3-thiazol-2-yl-urea | HCID 11415501 | — |
| Product | Cyclohex-3-enyl-cyclohexylamine | HCID 65702898 | — |
Reaction Steps
Cyclohex-3-enyl-cyclohexylamine was prepared by reductive amination of cyclohex-3-enylamine and cyclohexanone using general procedure (B). Reaction with carbonyl diimidazole and 2-aminothiazole using general procedure (A) gave the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08263634B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-2b43f48a32914de4a26ee08b26135aef |
| Source note | uspto-grants-2012_09 |