HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645523Generated: October 31, 2026
Potassium Carbonate → HCID 68706946, compound
https://huagongshe.com/reaction/645523
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | {spiro[2.5]octan-6-yl}methanamine hydrochloride | HCID 68704587 | — |
| Reactant | HCID 86627803 | HCID 86627803 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68706946 | HCID 68706946 | — |
Reaction Steps
To a solution of 4-[2-(5-benzylcarbamoyl-6-chloro-2-cyanopyrimidin-4-yloxy)ethyl]piperidine-1-carboxylic acid tert-butyl ester (0.23 mmol) in CH3CN (5 mL), C-spiro[2.5]oct-6-yl-methylamine hydrochloride (0.25 mmol) and K2CO3 (0.7 mmol) are added at room temperature. After warmed up to 70° C., the reaction mixture is stirred over night. The mixture is diluted with H2O and AcOEt, and extracted twice with AcOEt. The organic layer is dried over Na2SO4, filtered, and concentrated to give 4-(2-{5-benzylcarbamoyl-2-cyano-6-[(spiro[2.5]oct-6-ylmethyl)amino]pyrimidin-4-yloxy}ethyl)piperidine-1-carboxylic acid tert-butyl ester as a white solid; 1H-NMR (CDCl3), δ 0.17-0.30 (4H, m), 0.89-1.06 (4H, m), 1.14-1.38 (3H, m), 1.46 (9H, s), 1.49-1.79 (9H, m), 2.51 (2H, br t), 3.42 (2H, t), 4.00 (2H, m), 4.45 (2H, t), 4.55 (2H, d), 7.30-7.39 (5H, m), 8.12 (1H, t), 10.16 (1H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07704996B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-45dd79fcdb3e4fbcae9638e8227b413f |
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| Source note | uspto-grants-2010_04 |
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