HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 19936726, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 2-(5-Methylthien-2-yl)imidazo[2,1-b]benzothiazole-3-acetic acid | HCID 15233810 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19936726 | HCID 19936726 | — |
Reaction Steps
1.6 g (0.005 mole) of 2-(5-methylthien-2-yl)imidazo[2,1-b]-benzothiazole-3-acetic acid are treated, at room temperature, with 0.85 g (0.005 mole) of N,N'-carbonyldiimidazole in 30 ml of anhydrous tetrahydrofuran for 3 h 30 min. The mixture is cooled using an ice bath, an excess of ammonia in 10 ml of anhydrous tetrahydrofuran cooled to -10° C. is added, and the mixture is stirred for 4 h at room temperature. The solvent is evaporated under reduced pressure, the solid is collected by filtration, it is washed with water up to neutral pH, then with ethanol, and finally with ethyl ether. After recrystallization from methanol, 1 g of a beige compound is obtained. Melting point: 243°-245° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05418248 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-ae3db4f78f6546469875db280c67c323 |
| Source note | uspto-grants-1995_05 |