Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921145Generated: October 29, 2026

ethyl 7-(4-(((R)-5-(benzyloxy)hexyl)oxy)-4-methylpiperidin-1-yl)-6-((S)-1-(tert-butoxy)-2-ethoxy-2-oxoethyl)-5-methylpyrazolo[1,5-a]pyrimidine-2-carboxylate → ethyl 6-((S)-1-(tert-butoxy)-2-ethoxy-2-oxoethyl)-7-(4-(((R)-5-hydroxyhexyl)oxy)-4-methylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidine-2-carboxylate

https://huagongshe.com/reaction/921145

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 7-(4-(((R)-5-(benzyloxy)hexyl)oxy)-4-methylpiperidin-1-yl)-6-((S)-1-(tert-butoxy)-2-ethoxy-2-oxoethyl)-5-methylpyrazolo[1,5-a]pyrimidine-2-carboxylateHCID 118307152—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Productethyl 6-((S)-1-(tert-butoxy)-2-ethoxy-2-oxoethyl)-7-(4-(((R)-5-hydroxyhexyl)oxy)-4-methylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidine-2-carboxylateHCID 11830715682%

Reaction Steps

To a solution of ethyl 7-(4-(((R)-5-(benzyloxy)hexyl)oxy)-4-methylpiperidin-1-yl)-6-((S)-1-(tert-butoxy)-2-ethoxy-2-oxoethyl)-5-methylpyrazolo[1,5-a]pyrimidine-2-carboxylate (1.7 g, 2.55 mmol) in EtOH (25 mL) was added 10% Pd/C (0.271 g, 0.255 mmol) and the resulting mixture was stirred under balloon hydrogen atmosphere for 5 h. Mixture was then filtered and concentrated to afford ethyl 6-((S)-1-(tert-butoxy)-2-ethoxy-2-oxoethyl)-7-(4-(((R)-5-hydroxyhexyl)oxy)-4-methylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidine-2-carboxylate (1.2 g, 2.081 mmol, 82% yield) as viscous oil. LCMS (M+H)=577.3. Used as is in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273067B2
Source datasetuspto-grants-2016_03
ORD IDord-7f6fb772620f4b639d55cf0956df64e3
Source noteuspto-grants-2016_03