HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-(Sec-butylamino)thiazolo[5,4-b]pyridin-5-yl)methanol → 2-(Sec-butylamino)thiazolo[5,4-b]pyridine-5-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-(Sec-butylamino)thiazolo[5,4-b]pyridin-5-yl)methanol | HCID 86257065 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Sec-butylamino)thiazolo[5,4-b]pyridine-5-carbaldehyde | HCID 57527242 | — |
Reaction Steps
To a solution of (2-(sec-butylamino)thiazolo[5,4-b]pyridin-5-yl)methanol (0.1155 g, 0.487 mmol, 1.0 eq.) in THF (3.5 mL) under nitrogen was added MnO2 (0.6357 g, 7.3 mmol, 15.0 eq.). After 1 hr, the reaction solution was filtered through Celite and rinsed with THF. The filtrate was concentrated in vacuo to give crude 2-(sec-butylamino)thiazolo[5,4-b]pyridine-5-carbaldehyde as a colorless oil which was carried to the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07473784B2 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-43e49d607ffc4316b9911cfe20d6bbd2 |
| Source note | uspto-grants-2009_01 |