HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928558Generated: October 27, 2026
Triethylamine → [1-(2-Chloro-5-phenyl-thieno[2,3-d]pyrimidin-4-yl)-4-piperidyl]methanol
https://huagongshe.com/reaction/928558
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Piperidinemethanol | HCID 420771 | — |
| Reactant | 2,4-Dichloro-5-phenylthieno(2,3-d)pyrimidine | HCID 12724228 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | [1-(2-Chloro-5-phenyl-thieno[2,3-d]pyrimidin-4-yl)-4-piperidyl]methanol | HCID 89579549 | — |
Reaction Steps
4-Piperidinemethanol (987 mg, 8.57 mmol) was added to a stirred suspension of 2,4-dichloro-5-phenyl-thieno[2,3-d]pyrimidine (2 g, 7.14 mmol) and triethylamine (2.18 ml, 15.7 mmol) in dry ethanol (ml) at room temperature. Reaction was warmed to 40° C. and the resulting solution stirred for ˜2 h. Reaction was allowed to cool to room temperature and poured onto ice/water (50 ml). The resulting suspension was filtered and the solid dried in a vacuum oven at 40° C. The desired compound was obtained as a pale yellow solid (2.4 g, 93%). LCMS: (M+1) 360, RT=4.69 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290511B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-6253a31637214510b48cfecde35bbf41 |
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| Source note | uspto-grants-2016_03 |
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