HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281376Generated: October 31, 2026
Potassium Hydroxide → HCID 44247564, compound
https://huagongshe.com/reaction/2281376
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 57990318 | HCID 57990318 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 44247564 | HCID 44247564 | — |
| Product | HCID 57990269 | HCID 57990269 | — |
Reaction Steps
To a solution of 1-(4-(4-(4-(4-(aminomethyl)piperidin-1-yl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)phenyl)piperazin-1-yl)ethanone (60 mg, 0.10 mmol) in MeOH (3 mL), aq. 1N KOH (1 mL) was added. It was stirred at 60° C. for 3 h. After being concentrated in vacuo, the residue was acidified with HOAc (1 mL). The mixture was then purified by HPLC to give 4-(4-(aminomethyl)piperidin-1-yl)-N-(4-(piperazin-1-yl)phenyl)-7H-pyrrolo[2,3-d]pyrimidin-2-amine (3 mg) (MS 407.5 (M+H); UV 202.6, 269.9 nm) and 1-(4-(4-(4-(4-(aminomethyl)piperidin-1-yl)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)phenyl)piperazin-1-yl)ethanone (15 mg) (MS 449.5 (M+H); UV 202.6, 273.4 nm).
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-42f8989691a34825a8d19e69897d115f |
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| Source note | uspto-grants-2015_09 |
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