HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916122Generated: November 3, 2026
Ammonium Hydroxide → HCID 131731114, compound
https://huagongshe.com/reaction/1916122
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 69815196 | HCID 69815196 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 131731114 | HCID 131731114 | — |
Reaction Steps
In a 10 mL sealed tube {2-methanesulfonyl-5-[5-(2-trimethysilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazin-2-yl]-pyrimidin-4-yl}-[(S)-1-(2-methyl-propane-1-sulfonyl)-piperidin-3-yl]-amine (38 mg, 609 μmol) and ammonium hydroxide (450 mg, 0.5 ml, 12.8 mmol) were combined with 1,4-dioxane (2 ml) to give a light yellow solution. The reaction mixture was heated to 90° C. and stirred for 6 h. It was concentrated and diluted with water, extracted with ethyl acetate (2×20 ml). The organic layers were dried (MgSO4) and concentrated to give N*4*-[(S)-1-(2-methyl-propane-1-sulfonyl)-piperidin-3-yl]-5-[5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazin-2-yl]-pyrimidine-2,4-diamine as a yellow foaming solid. MS (ES+): 561.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618103B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-9300cd6124cc4fb988d82ea1c00a8542 |
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| Source note | uspto-grants-2013_12 |
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