HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 6-[(S)-4-(4-Chloro-phthalazin-1-yl)-3-methyl-piperazin-1-yl]-nicotinic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,4-Dichlorophthalazine | HCID 78490 | — |
| Reactant | 6-((S)-3-Methyl-piperazin-1-yl)-nicotinic acid ethyl ester | HCID 57471615 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 6-[(S)-4-(4-Chloro-phthalazin-1-yl)-3-methyl-piperazin-1-yl]-nicotinic acid ethyl ester | HCID 59240681 | 30.3% |
Reaction Steps
A solution of 6-((S)-3-methyl-piperazin-1-yl)-nicotinic acid ethyl ester (1.0 g, 4.0 mmol, 1 eq), 1,4-dichlorophthalazine (840 mg, 4.2 mmol, 1.05 eq) and triethyl amine (3.9 g, 2.8 mL, 38 mmol, 9.5 eq) in NMP (8 mL) is heated at 100 C for 26 h. Reaction is diluted with water (15 mL) and extracted with EtOAc (3×25 mL). The combined organic fractions are dried over magnesium sulfate, concentrated and purified by silica gel chromatography (5-50% EtOAc/Heptane) to yield the desired compound (500 mg, 30% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08536168B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-982eee3b37a14de48eded3e20b948774 |
| Source note | uspto-grants-2013_09 |