HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238228Generated: October 30, 2026
Potassium Iodide → HCID 68800627, compound
https://huagongshe.com/reaction/238228
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Amino-1-Boc-piperidine | HCID 1268291 | — |
| Reactant | HCID 59993195 | HCID 59993195 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68800627 | HCID 68800627 | — |
Reaction Steps
A mixture of 2-(1-bromo-ethyl)-3-methyl-3H-quinazolin-4-one (801 mg, 3 mmol), 4-amino-1-N-Boc piperidine (661 mg, 3.3 mmol), potassium iodide (498 mg, 3 mmol) and potassium carbonate (622 mg, 4.5 mmol) in acetonitrile (12 mL) was heated at 65° C. for 3 days. The reaction mixture was then concentrated in vacuo. The residue was dissolved in dichloromethane and washed with saturated sodium thiosulphate solution and water. The organic layer was dried over magnesium sulfate and concentrated in vacuo to yield 4-[1-(3-Methyl-4-oxo-3,4-dihydro-quinazolin-2-yl)-ethylamino]-piperidine-1-carboxylic acid tert-butyl ester (HPLC ret. time 2.20, 10-99% CH3CN, 5 min run, ESI-MS m/z 387.4 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642609B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-dee036ede34548e996bcb3bc2996c22f |
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| Source note | uspto-grants-2014_02 |
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