HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(4-Ethoxy-5-methylcarbamoylpyridin-2-ylmethyl)-N'-(fluoren-9-ylmethyloxycarbonyl)thiourea → 9H-Fluoren-9-ylmethyl (7-ethoxy-6-methylcarbamoyl-2H-imidazo[1,5-a]pyridin-3-ylidene)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(4-Ethoxy-5-methylcarbamoylpyridin-2-ylmethyl)-N'-(fluoren-9-ylmethyloxycarbonyl)thiourea | HCID 57791308 | — |
| Catalyst | Mercury bis(trifluoroacetate) | HCID 2723924 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 9H-Fluoren-9-ylmethyl (7-ethoxy-6-methylcarbamoyl-2H-imidazo[1,5-a]pyridin-3-ylidene)carbamate | HCID 178465836 | — |
Reaction Steps
875 mg of N-(4-ethoxy-5-methylcarbamoyl pyridin-2-ylmethyl)-N′-(fluoren-9-ylmethyloxycarbonyl)thiourea (Example 19a, crude product) were dissolved in 25 ml of dioxane and treated at RT with 837 mg (1.96 mmol) of mercury(II) trifluoroacetate. After 10 minutes, the mixture was concentrated and the residue was taken up in DCM. The organic phase was washed three times with 4% strength LiCl solution and once with water, dried with MgSO4 and concentrated in a rotary evaporator. The crude product thus obtained (590 mg) was reacted further without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07863269B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-8b381985904d458e8891b45a0d720ba1 |
| Source note | uspto-grants-2011_01 |