HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Acetylpiperazine → (4-Acetyl-piperazin-1-yl)pyridin-3-yl-acetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Acetylpiperazine | HCID 83795 | — |
| Reactant | Ethyl 2-bromo-2-(pyridin-3-yl)acetate | HCID 21985933 | — |
| Product | (4-Acetyl-piperazin-1-yl)pyridin-3-yl-acetic acid ethyl ester | HCID 69849407 | 60% |
Reaction Steps
N-acetyl-piperazine (3.7 g; 28.8 mmol; 2.8 equiv) was combined with bromo-pyridin-3-yl-acetic acid ethyl ester (approx. 2.5 g; 10 mmol). Purification on a 3×16 cm silica column using a 30% then 40% ethyl acetate/hexanes (v/v) mobile phase followed by a 2% methanol/dichloromethane (v/v) mobile phase resulted in 1.84 g light yellow oil (approx. 60% yield). MS(ES) calc'd: [M+H]+=292.2 m/z; [M+Na]+=314.2 m/z.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06743794B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-5f7765389b5b496bb3641e9d3af6995f |
| Source note | uspto-grants-2004_06 |