HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazo(4,3-b)(1,3)thiazole-7-carbaldehyde → 7-[(5-Methylthiopyridin-3-yl)hydroxymethyl]imidazo[5,1-b]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazo(4,3-b)(1,3)thiazole-7-carbaldehyde | HCID 22390357 | — |
| Reactant | 3-Bromo-5-(methylthio)pyridine | HCID 22390359 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Product | 7-[(5-Methylthiopyridin-3-yl)hydroxymethyl]imidazo[5,1-b]thiazole | HCID 22390316 | 64% |
Reaction Steps
7-[(5-Methylthiopyridin-3-yl)hydroxymethyl]imidazo-[5,1-b]thiazole (119 mg) was prepared in substantially the same manner as in step a) of Synthesis Example 5, except that 204 mg of 3-bromo-5-methylthiopyridine, 0.656 ml of a 1.6 N n-butyllithium/n-hexane solution, and 102 mg of 7-formylimidazo[5,1-b]thiazole were used as the starting materials.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06908913B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-c30938443d744290a16789e492312dee |
| Source note | uspto-grants-2005_06 |