HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-Ethylthiazolo[4,5-c]quinolin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | n-(2-Ethylthiazolo[4,5-c]quinolin-4-yl)trichloroacetamide | HCID 22648275 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Ethylthiazolo[4,5-c]quinolin-4-amine | HCID 9964620 | — |
Reaction Steps
N-(2-ethylthiazolo[4,5-c]quinolin-4-yl)trichloroacetamide (0.40 g) was suspended in a solution of ammonia in methanol (20 mL of 2M) and then stirred at ambient temperature for 30 minutes. The reaction mixture was concentrated under vacuum. The residue was washed with water and then dried to provide 0.19 g of crude product which was recrystallized from ethyl acetate/hexane to provide 2-ethylthiazolo[4,5-c]quinolin-4-amine as tan needles, m.p. 170-172° C. Analysis: Calculated for C12H11N3S: % C, 62.85; % H, 4.83; % N, 18.32; Found: % C, 62.58; % H, 4.78; % N, 18.08.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06110929 |
| Source dataset | uspto-grants-2000_08 |
| ORD ID | ord-430a3265a09744639ca8e2a7e8d90e87 |
| Source note | uspto-grants-2000_08 |