HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 136162347, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 178483580 | HCID 178483580 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 136162347 | HCID 136162347 | — |
Reaction Steps
500 mg (1.18 mmol) of 1-{3-[5-(3-dimethylaminopropoxy)pyrimidin-2-yl]-benzyl}-N-hydroxy-6-oxo-1,6-dihydropyridazine-3-carboxamidine are dissolved in 15 ml of DMF, and 286 μl (3.54 mmol) of pyridine are added. 124 μl (1.30 mmol) of ethyl chloroformate are subsequently added with stirring, and the solution is stirred at 80° C. for 15 and subsequently at 100° C. for 72 h. The reaction mixture is evaporated, and the residue is purified by means of preparative HPLC; yield: 21.2 mg of “A227” trifluoroacetate; HPLC: Rt=2.07 min; LC-MS: 450 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09284300B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-60f0b3d03cdf4b7781fed433bf912c53 |
| Source note | uspto-grants-2016_03 |