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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Piperidinol, 1-methyl- | HCID 66048 | — |
| Reactant | HCID 178501306 | HCID 178501306 | — |
| Product | HCID 117598855 | HCID 117598855 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328138B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-8c4810515e6449669883e1ed454983c4 |
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| Source note | uspto-grants-2016_05 |
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