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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773605Generated: November 1, 2026

HCID 66664639, compound → HCID 66665016, compound

https://huagongshe.com/reaction/1773605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66664639HCID 66664639—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 66665016HCID 6666501664.6%

Reaction Steps

A mixture of (1-{6-[(6-benzyloxy-pyrazolo[1,5-a]pyrimidine-3-carbonyl)-amino]-quinolin-7-yl}-piperidin-4-ylmethyl)-carbamic acid tert-butyl ester (0.4 g) and palladium on carbon (10%, 50 mg) in ethanol (20 mL) was stirred under hydrogen atmosphere (balloon pressure) for 2 days. The resulting mixture was filtered over a CELITE™ pad and the filtrate was evaporated under reduced pressure. The crude residue was purified by flash chromatography to afford 0.220 g of (1-{6-[(6-hydroxy-pyrazolo[1,5-a]pyrimidine-3-carbonyl)-amino]-quinolin-7-yl}-piperidin-4-ylmethyl)-carbamic acid tert-butyl ester as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255110B2
Source datasetuspto-grants-2016_02
ORD IDord-0093e0e68ada4535a0d676128de4c93b
Source noteuspto-grants-2016_02