HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → HCID 24876135, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Tert-Butyl isocyanide | HCID 23577 | — |
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | HCID 87217901 | HCID 87217901 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 24876135 | HCID 24876135 | 34.2% |
Reaction Steps
A solution of 380 mg (3.8 mmol) 2-amino-thiazole, 749 mg (3.8 mmol) 5-(pyridine-2-yl-ethynyl)-furan-2-carbaldehyde, 378 mg (3.8 mmol) tert.butyl-isonitril and 73 μl of a 70% aq. perchloric acid in chloroform (2 ml) was heated to 45° C. while being stirred for 16 h. Dilution with DCM was subsequently performed and a 1 molar aq. Na2CO3 sol. was added. After 10 min of stirring at RT, the phases were separated. The aqueous phase was extracted with DCM. The collected organic phases were dried over Na2SO4, filtered and concentrated in a vacuum. 472 mg (1.3 mmol, 34%) N-tert-butyl-6-(5-(pyridine-2-ylethynyl)furan-2-yl)imidazo[2,1-b]thiazole-5-amine was obtained by CC (AE) with the residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07893069B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-44ffb026b87549be8c5962a9ad703445 |
| Source note | uspto-grants-2011_02 |