HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzoylpiperazine → HCID 59693829, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzoylpiperazine | HCID 762654 | — |
| Reactant | HCID 67152743 | HCID 67152743 | — |
| Product | HCID 59693829 | HCID 59693829 | — |
Reaction Steps
Precursor 5p, 1-benzoyl-4-[(7-chloro-4-azaindol-3-yl)-oxoacetyl]piperazine was prepared by the same method as Precursor 5a starting from Potassium (7-chloro-4-fluoro-4-azaindol-3-yl)oxoacetate, Precursor 4e, and 1-benzoyl-piperazine. 1H NMR (500 MHz, CD3OD) δ8.83 (s, 1H), 8.63 (d, 1H, J=5.35 Hz), 7.91 (d, 1H, J=5.75 Hz), 7.47 (m, 5H), 3.80-3.30 (m, 3H). MS m/z: (M+H)+ Calc'd for C20H18ClN4O3: 397.11; Found 397.02. HPLC retention time: 1.20 minutes (column A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07501420B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-3a278e3741de400eb1c76860d7c67d07 |
| Source note | uspto-grants-2009_03 |