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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522400Generated: October 31, 2026

4-Piperidinol, 1-methyl- → HCID 117598855, compound

https://huagongshe.com/reaction/522400

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Piperidinol, 1-methyl-HCID 66048—
ReactantHCID 178501306HCID 178501306—
ProductHCID 117598855HCID 117598855—

Reaction Conditions

Temperature40 °C

Reaction Steps

Methyl (1aR,55,8S,10R,22aR)-5-tert-butyl-17-hydroxy-3,6-dioxo-1,1a,3,4,5,6,9,10,18,19,20,21,22,22a-tetradecahydro-8H-7,10-methanocyclopropa[18,19][1,10,3,6]dioxadiazacyclononadecino[11,12-b]quinoline-8-carboxylate synthesized in example 113, step 5 was reacted with 1-methylpiperidin-4-ol using the procedure described for Example 137 (heating was required: 40° C. for 18 hours). LRMS (ES+) m/z 651.55 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328138B2
Source datasetuspto-grants-2016_05
ORD IDord-8c4810515e6449669883e1ed454983c4
Source noteuspto-grants-2016_05