HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-[[5-(t-Butyldimethylsilyloxymethyl)pyridin-3-yl]hydroxymethyl]imidazo[5,1-b]thiazole → 7-[5-(t-Butyldimethylsilyloxymethyl)pyridin-3-yl]carbonyl imidazo[5,1-b]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-[[5-(t-Butyldimethylsilyloxymethyl)pyridin-3-yl]hydroxymethyl]imidazo[5,1-b]thiazole | HCID 22390377 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-[5-(t-Butyldimethylsilyloxymethyl)pyridin-3-yl]carbonyl imidazo[5,1-b]thiazole | HCID 22390284 | 89.1% |
Reaction Steps
Manganese dioxide (1.43 g) was added to a solution of 803 mg of 7-[[5-(t-butyldimethylsilyloxymethyl)-pyridin-3-yl]hydroxymethyl]imidazo[5,1-b]thiazole in 10 ml of dichloromethane, and the mixture was stirred at room temperature for 16 hr. The reaction solution was filtered through Celite, followed by washing with dichloromethane. The filtrate was concentrated under the reduced pressure to give 712 mg of 7-[5-(t-butyldimethylsilyloxymethyl)pyridin-3-yl]carbonyl imidazo[5,1-b]thiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06908913B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-20d8ab6d72b540d5b289ff25c300ee82 |
| Source note | uspto-grants-2005_06 |