HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 6-Chloro-4-(5,6-dimethoxypyridin-2-ylamino)pyridazine-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 6-Chloro-4-(5,6-dimethoxy-pyridin-2-ylamino)-pyridazine-3-carboxylic acid methyl ester | HCID 86689745 | — |
| Product | 6-Chloro-4-(5,6-dimethoxypyridin-2-ylamino)pyridazine-3-carboxamide | HCID 86689746 | 96% |
Reaction Steps
6-Chloro-4-(5,6-dimethoxy-pyridin-2-ylamino)-pyridazine-3-carboxylic acid methyl ester (1.7 g, 5.2 mmol) was suspended in ammonia in methanol (7N, 30.0 mL, 210 mmol) and the flask sealed. After stirring for 6 h at room temperature the mixture was concentrated in vacuo to give 6-chloro-4-(5,6-dimethoxy-pyridin-2-ylamino)-pyridazine-3-carboxylic acid amide (1.55 g, 96%) as a yellow powder. LC-MS: 310.4 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08901124B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-32ddf3bdf38c4758903de376dd82782e |
| Source note | uspto-grants-2014_12 |