HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908123Generated: October 26, 2026
Hydrochloric Acid → HCID 25258354, compound
https://huagongshe.com/reaction/908123
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 25258351 | HCID 25258351 | — |
| Reactant | HCID 178508814 | HCID 178508814 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 25258354 | HCID 25258354 | 65% |
Reaction Steps
To a solution of methyl {5-[4-(2-bromo-2-methylpropanoyl)phenyl]bicyclo[3.2.2]non-1-yl}acetate (Intermediate 24; 80 mg, 0.19 mmol) in absolute EtOH (20 mL) was added 5,6-diaminopyrimidin-4-ol (30 mg, 0.21 mmol) followed by 1M HCl (0.21 mL). The suspension was heated under gentle reflux (80° C.) overnight then allowed to cool, the solvent removed and the residue treated with 2M NaOH (2 mL). The aqueous phase was extracted into EtOAc (3×50 mL), the organic extracts were combined, dried (MgSO4) and concentrated to leave a pale yellow gum. This was purified on a 12 g Crawford silicycle cartridge, loading in DCM and eluting with 0-5-10% MeOH-DCM, giving the title compound as a pale yellow gum (55 mg, 0.123 mmol, 65%); 1H NMR (CDCl3) 1.41-1.61 (14H, m), 1.71 (6H, s), 2.07 (2H, s), 3.61 (3H, s), 7.11 (2H, d), 7.51 (2H, d), 8.14 (1H, s); MS m/e MH+ 449.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08017603B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-100b935434144e0fac01415320555d04 |
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| Source note | uspto-grants-2011_09 |
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