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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035479Generated: October 27, 2026

Aminoammonium hydroxide → 4-(3-aminopropyl)-6-[5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]pyrimidin-2-ylamine

https://huagongshe.com/reaction/1035479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminoammonium hydroxideHCID 44558531—
Reactant2-(3-{2-amino-6-[5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-pyrimidin-4-yl}propyl)isoindole-1,3-dioneHCID 58217090—
SolventMethanolHCID 887—
Product4-(3-aminopropyl)-6-[5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]pyrimidin-2-ylamineHCID 25165367—

Reaction Conditions

Temperature60 °C

Reaction Steps

8.6 0.003 ml (0.06 mmol) of hydrazinium hydroxide is added at RT to a solution of 29 mg (0.06 mmol) of 2-(3-{2-amino-6-[5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl}pyrimidin-4-yl]propyl)isoindole-1,3-dione in 0.5 ml of methanol. The reaction solution is heated for 5 min at 60° C. in the microwave. The reaction mixture is evaporated in vacuo, and the residue is purified by preparative HPLC, giving 4-(3-aminopropyl)-6-[5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]pyrimidin-2-ylamine as yellow solid, ESI 349

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546390B2
Source datasetuspto-grants-2013_10
ORD IDord-3a98608fc24e41e994e882847fe3373c
Source noteuspto-grants-2013_10