HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281379Generated: November 1, 2026
Potassium Hydroxide → HCID 44467741, compound
https://huagongshe.com/reaction/2281379
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 57990284 | HCID 57990284 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 44467741 | HCID 44467741 | — |
| Product | HCID 44467742 | HCID 44467742 | — |
Reaction Steps
To a solution of (S)-1-(4-(4-(4-(3-hydroxypyrrolidin-1-yl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)phenyl)piperazin-1-yl)ethanone (80 mg, 0.14 mmol) in MeOH (3 mL), aq. 1N KOH (1 mL) was added. It was stirred at 60° C. for 4 h. After being concentrated in vacuo, the residue was acidified with HOAc (1 mL). The mixture was then purified by HPLC to give (S)-1-(2-(4-(piperazin-1-yl)phenylamino)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrrolidin-3-ol (5 mg) (MS 380.5 (M+H)) and (S)-1-(4-(4-(4-(3-hydroxypyrrolidin-1-yl)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)phenyl)piperazin-1-yl)ethanone (20 mg) (MS 422.5 (M+H)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139581B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-0bd752afdd024c0f992f76f77cf87cf5 |
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| Source note | uspto-grants-2015_09 |
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