HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225489Generated: October 30, 2026
Hydrochloric Acid → HCID 69071303, compound
https://huagongshe.com/reaction/225489
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 69070115 | HCID 69070115 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69071303 | HCID 69071303 | — |
Reaction Steps
3.65 ml of THF solution with 1.0M diisobutylaluminum hydride was added dropwise under ice cooling into a mixture of 400 mg of ethyl 4-[2-(4-chloro-2,5-difluorophenyl)thieno[3,2-d]pyrimidine-4-yl]piperazine-2-carboxylate and 10 ml of THF and the resultant was stirred for 3 hours at room temperature. After 10 ml of 1M HCl aq was added to the reaction mixture and stirred for 10 minutes at room temperature, 20 ml of 1M NaOH aq was added and extracted with chloroform. After the organic layer was dried over anhydrous magnesium sulfate, the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform-MeOH) to give an oily substance. After the obtained oily substance was dissolved in 10 ml of THF and 1 ml of 4M HCl-dioxane solution was added, the resultant was concentrated under reduced pressure to give a solid. This solid washed with EtOH-ether to give 60 mg of {4-[2-(4-chloro-2,5-difluorophenyl)thieno[3,2-d]pyrimidine-4-yl]piperazine-2-yl}methanol dihydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557112B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-e4496eaa8db248de9003204aac596465 |
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| Source note | uspto-grants-2009_07 |
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