HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353161Generated: October 30, 2026
Phenyl glycidyl ether → HCID 11678721, compound
https://huagongshe.com/reaction/2353161
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenyl glycidyl ether | HCID 31217 | — |
| Reactant | HCID 57494060 | HCID 57494060 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11678721 | HCID 11678721 | — |
Reaction Steps
Treatment of 4-[2-(1H-indazol-4-yl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl]-piperazine-1-carboxylic acid tert-butyl ester with HCl in DCM/MeOH yielded 2-(1H-indazol-4-yl)-4-morpholin-4-yl-6-piperazin-1-ylmethyl-thieno[3,2-d]pyrimidine. A mixture of 2-(1H-indazol-4-yl)-4-morpholin-4-yl-6-piperazin-1-ylmethyl-thieno[3,2-d]pyrimidine (150 mg) and 1,2-epoxy-3-phenoxypropane (40 mg) was suspended in 50% DMF/0.1M sodium phosphate buffer (2 mL) and shaken at 55° C. overnight. After stirring for 24 h the reaction mixture was then diluted with DCM, washed with brine, dried (MgSO4) and the solvent removed in vacuo. The residue was purified by flash chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07750002B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-c9772035dd3e43e9b8ba4e24e22cdbc6 |
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| Source note | uspto-grants-2010_07 |
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