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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900326Generated: October 31, 2026

tert-butyl 1-((4-(1-(3-fluorobenzyl)-1H-indazol-5-ylamino)quinazolin-5-yl)methyl)piperidin-4-ylcarbamate → N-(1-(3-fluorobenzyl)-1H-indazol-5-yl)-5-((4-aminopiperidin-1-yl)methyl)quinazolin-4-amine

https://huagongshe.com/reaction/900326

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 1-((4-(1-(3-fluorobenzyl)-1H-indazol-5-ylamino)quinazolin-5-yl)methyl)piperidin-4-ylcarbamateHCID 58711715—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
ProductN-(1-(3-fluorobenzyl)-1H-indazol-5-yl)-5-((4-aminopiperidin-1-yl)methyl)quinazolin-4-amineHCID 5871171988.3%

Reaction Steps

21A (52 mg, 0.089 mmoL) was dissolved in a mixture of TFA/DCM (2 ml/2 ml) and stirred at rt for 10 min, then concentrated. The residue was purified by prep HPLC to give 21B (38 mg, 88%). It has an analytical HPLC retention time=1.93 min (Chromolith SpeedROD column 4.6×50 mm, 10-90% aqueous methanol containing 0.1% TFA over 4 minutes, 4 mL/min, monitoring at 254 nm) and a LC/MS M++H=482+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07358256B2
Source datasetuspto-grants-2008_04
ORD IDord-7a3961c07b14484392f1f68b9762696a
Source noteuspto-grants-2008_04