HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Ethylpiperazine → 5-Chloro-4-(4-ethylpiperazin-1-yl)-3-nitropyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Ethylpiperazine | HCID 79196 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Amino-4,5-dichloro-3-nitropyridine | HCID 46867660 | — |
| Reactant | 2-(4-(2-amino-5-bromo-3-nitropyridin-4-yl)piperazin-1-yl)-N-(thiazol-2-yl)acetamide | HCID 46867803 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 5-Chloro-4-(4-ethylpiperazin-1-yl)-3-nitropyridin-2-amine | HCID 57897153 | 31% |
Reaction Steps
This was prepared using the same procedure as for 2-(4-(2-amino-5-bromo-3-nitropyridin-4-yl)piperazin-1-yl)-N-(thiazol-2-yl)acetamide, but here using 4,5-dichloro-3-nitropyridin-2-amine (75 mg, 0.36 mmol), iPrOH (2 mL), DIPEA (3.5 eq, 1.26 mmol, 0.22 mL) and 1-ethylpiperazine (1.2 eq, 0.43 mmol, 0.05 mL). Concentration in vacuo and purification by preparative tlc (CH2Cl2-MeOH, 95:5) gave the product (32 mg, 31%) as a yellow solid;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088761B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-6d8ce21d3d684d39bd7600be43ef4a93 |
| Source note | uspto-grants-2012_01 |