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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783581Generated: October 30, 2026

HCID 59693877, compound → HCID 59694060, compound

https://huagongshe.com/reaction/1783581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59693877HCID 59693877—
ReactantHCID 59915963HCID 59915963—
ProductHCID 59694060HCID 59694060—

Reaction Steps

Precursor 5o, (R)-1-picolinoyl-3-methyl-4-[(7-bromo-4-fluoro-6-azaindol-3-yl)-oxoacetyl]piperazine was prepared by the same method as Precursor 5a starting from Potassium (7-bromo-4-fluoro-6-azaindol-3-yl)oxoacetate, Precursor 4h, and (R)-3-methyl-1-picolinoyl-piperazine. 1H NMR (500 MHz, CD3OD) δ8.68-7.52 (m, 6H), 4.94-2.69 (m, 7H), 1.48-1.24 (m, 3H). MS m/z: (M+H)+ Calc'd for C20H18BrFN5O3: 474.06; Found 474.23. HPLC retention time: 1.20 minutes (column A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501420B2
Source datasetuspto-grants-2009_03
ORD IDord-2670d46ed5f94f8285d775264343c7db
Source noteuspto-grants-2009_03