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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052987Generated: October 30, 2026

Hydrazine hydrate (1:1) → HCID 178511295, compound

https://huagongshe.com/reaction/2052987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 178508598HCID 178508598—
SolventEthanolHCID 702—
ProductHCID 178511295HCID 178511295—

Reaction Steps

To a solution of 4.15 g (7.83 mmol) of trans-2-{3-[4-amino-5-(3-benzyloxy-phenyl)-pyrrolo[2,3-d]pyrimidin-7-yl]-cyclobutylmethyl}-isoindole-1,3-dione in 100 ml of dry ethanol are added dropwise at RT and under argon 5.87 g (5.7 ml; 117.5 mmol) of hydrazine monohydrate. After 20 min all the starting material is dissolved, and the reaction is complete after 20 h stirring at RT. The colorless precipitate is filtered off, and washed with ethanol. The filtrate is evaporated to dryness and the crude compound is purified by chromatography on silica gel (dichloromethane:methanol:NH4OHaqu.=90:10:1) to provide trans-7-(3-aminomethyl-cyclobutyl)-5-(3-benzyloxy-phenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-ylamine. Analytical HPLC: tR=7.50 min (Grad 1); ES-MS: m/eo=400; 1H-NMR (CDCl3): 8.30/s (1H); 7.3-7.5/m (6H); 7.20/s (1H); 7.05-7.15/2 peaks (2H); 6.99/m (1H); 5.41/m (1H); 5.14/s (2H); 5.04/broad s (2H); 2.98/d (2H); 2.54-2.69/m (2H); 2.35-2.54/m (3H); 1.73/broad s (2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326699B2
Source datasetuspto-grants-2008_02
ORD IDord-994d9e63accf4c5ca63fa30a3c213632
Source noteuspto-grants-2008_02