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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052985Generated: October 30, 2026

Hydrazine hydrate (1:1) → HCID 178511294, compound

https://huagongshe.com/reaction/2052985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 178508597HCID 178508597—
SolventEthanolHCID 702—
ProductHCID 178511294HCID 178511294—

Reaction Steps

To a solution of 3.84 g (7.25 mmol) of cis-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 3.75 g (3.64 ml; 74.96 mmol) of hydrazine monohydrate. After 2 h most of the starting material is not yet dissolved, and additional 1.6 ml of hydrazine monohydrate are added thereto (total amount: 14.8 equivalents). The reaction is complete after 20 h. 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 silicagel (dichloromethane:methanol:aqueous concentrated ammonia=90:10:1) to provide cis-7-(3-aminomethyl-cyclobutyl)-5-(3-benzyloxy-phenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-ylamine. Analytical HPLC: tR=7.47 min (Grad 1); ES-MS: m/eo=400; 1H-NMR (CDCl3): 8.31/s (1H); 7.3-7.5/m (6H); 7.12/s (1H); 7.05-7.08/2 peaks (2H); 6.99/m (1H); 5.17/m (1H); 5.14/s (2H); 5.04/broad s (2H); 2.87/d (2H); 2.75-2.65/m (2H); 2.2-2.1/m (2H); 1.55/broad s (2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326699B2
Source datasetuspto-grants-2008_02
ORD IDord-2c11fc116023443d9c9c82598d19a6cc
Source noteuspto-grants-2008_02