HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(3-chloro[1,2,4]triazolo[4,3-b]pyridazin-6-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
| Reactant | 3-Chloro-[1,2,4]triazolo[4,3-b]pyridazin-6-amine | HCID 67524192 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(3-chloro[1,2,4]triazolo[4,3-b]pyridazin-6-yl)acetamide | HCID 67524510 | — |
Reaction Steps
0.11 cm3 of acetic anhyhdride is added to a mixture of 202 mg of 3-chloro[1,2,4]triazolo[4,3-b]pyridazin-6-amine in 5 cm3 of pyridine at 0° C. The temperature is allowed to rise to 20° C. over 6 h, then 0.05 cm3 of acetic anhydride is again added and stirring is maintained for 24 h. The precipitate formed is spin-filter-dried and then washed with ethyl ether and pentane. This solid is purified by chromatography on Biotage Quad 12/25 (KP-SIL, 60 A; 32-63 μM), elution being carried out with a gradient of dichloromethane/methanol of 100/0 to 90/10. 41 mg of N-(3-chloro[1,2,4]triazolo[4,3-b]pyridazin-6-yl)acetamide are thus obtained in the form of a white powder, the characteristics of which are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115134B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-746a850dcfc34738b4e25b0cec2aee82 |
| Source note | uspto-grants-2015_08 |