HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916125Generated: November 3, 2026
Ammonium Hydroxide → HCID 58177247, compound
https://huagongshe.com/reaction/1916125
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 58177355 | HCID 58177355 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 58177247 | HCID 58177247 | — |
Reaction Steps
A suspension of ((S)-1-methanesulfonyl-piperidin-3-yl)-{2-methanesulfonyl-5-[5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazin-2-yl]-pyrimidin-4-yl}-amine from Example 84, step 1 in ammonium hydroxide in dioxane was heated at 90° C. for 6 hours. The reaction was concentrated and diluted with water and extracted with EtOAc (2×20 ml). The organic layers were dried over MgSO4 and concentrated in vacuo to give a yellow foaming solid. MS (ES+): 561. The de-protection step was similar to step 5 of Example 76 to give N*4*-((S)-1-methanesulfonyl-piperidin-3-yl)-5-(5H-pyrrolo[2,3-b]pyrazin-2-yl)-pyrimidine-2,4-diamine. MS (ES+): 389.
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-cb6cfb07e0ae4037944de5b5116f90e1 |
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| Source note | uspto-grants-2013_12 |
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