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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916125Generated: November 3, 2026

Ammonium Hydroxide → HCID 58177247, compound

https://huagongshe.com/reaction/1916125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 58177355HCID 58177355—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 58177247HCID 58177247—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618103B2
Source datasetuspto-grants-2013_12
ORD IDord-cb6cfb07e0ae4037944de5b5116f90e1
Source noteuspto-grants-2013_12