HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594662Generated: November 4, 2026
p-Toluenesulfonic acid → HCID 69084124, compound
https://huagongshe.com/reaction/594662
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Triethyl orthoacetate | HCID 66221 | — |
| Reactant | HCID 69081808 | HCID 69081808 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 69084124 | HCID 69084124 | — |
Reaction Steps
A mixture of 6-(3-amino-2-hydroxy-6-methoxyphenyl)-1-(quinolin-2-ylmethyl)piperidin-2-one (100 mg; 0.26 mmol), commercially available p-TsOH (2 mg; 0.01 mmol), and commercially available triethyl orthoacetate (290 mg; 1.69 mmol) was refluxed (100° C.) for 25 min. After cooling to rt, AcOEt was added, and the obtained mixture was filtered over a pad of celite. The filtrate was then washed with water and brine, and the mixed aq. layers were further extracted with AcOEt. The mixed organic layers were then dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure. Subsequent purification by FC (DCM/MeOH=20/1) afforded the target compound. LC-MS (conditions A): tR=0.54 min.; [M+H]+: 401.73 g/mol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242970B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-4a12fcf9d4444a1cbf5b2488aa70fb8f |
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| Source note | uspto-grants-2016_01 |
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