HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 59693965, compound → HCID 59693890, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 59693965 | HCID 59693965 | — |
| Reactant | HCID 67152700 | HCID 67152700 | — |
| Product | HCID 59693890 | HCID 59693890 | — |
Reaction Steps
Precursor 5n, (S)-1-picolinoyl-3-methyl-4-[(7-bromo-6-azaindol-3-yl)-oxoacetyl]piperazine was prepared by the same method as Precursor 5a starting from Potassium (7-bromo-6-azaindol-3-yl)oxoacetate, Precursor 4g, and (S)-3-methyl-1-picolinoyl-piperazine. 1H NMR (500 MHz, CDCl3) δ 8.63-7.36 (m, 7H), 5.02-3.06 (m, 7H), 1.42-1.26 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07501420B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-1eb79520a9784ba1af23dffd3379eb93 |
| Source note | uspto-grants-2009_03 |