HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → HCID 11415501, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Bis-(1H-imidazol-2-YL)-methanone | HCID 5250894 | — |
| Reactant | HCID 13040867 | HCID 13040867 | — |
| Product | HCID 11415501 | 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 | USRE045183E1 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-0fbd4833d18f44739bba5e40aa23bd38 |
| Source note | uspto-grants-2014_10 |