HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510967Generated: October 30, 2026
6-chloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine → tert-Butyl 4-[3-chloro-6-methoxy-2-methyl-5-(1-{[9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-yl]amino}ethyl)phenyl]piperidine-1-carboxylate
https://huagongshe.com/reaction/510967
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-chloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine | HCID 97740 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Tert-butyl 4-{3-[1-aminoethyl]-5-chloro-2-methoxy-6-methylphenyl}piperidine-1-carboxylate | HCID 86666879 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | tert-Butyl 4-[3-chloro-6-methoxy-2-methyl-5-(1-{[9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-yl]amino}ethyl)phenyl]piperidine-1-carboxylate | HCID 86666880 | 109% |
Reaction Steps
A mixture of tert-butyl 4-{3-[1-aminoethyl]-5-chloro-2-methoxy-6-methylphenyl}piperidine-1-carboxylate (150 mg, 0.392 mmol), 6-chloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine (122 mg, 0.509 mmol), and sodium bicarbonate (35 mg, 0.41 mmol) in 1-butanol (4.7 mL) was degassed with N2 for ˜5 minutes. The mixture was heated at 110° C. for 3 h under nitrogen. The solvent was removed under reduced pressure and the resulting residue was diluted with EtOAc, washed with sat. NaHCO3, water, brine, dried over Na2SO4, filtered and concentrated. The residue was purified by chromatography eluting with 0 to 80% EtOAc in CH2Cl2 to provide the desired product (0.25 g). LCMS calculated for C30H42ClN6O4 (M+H)+: m/z=585.3. found: =585.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096600B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-146b50aea01d40459055e915bf37592a |
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| Source note | uspto-grants-2015_08 |
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