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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864518Generated: November 1, 2026

3-Aminoazetidine, 3-BOC protected → HCID 60208257, compound

https://huagongshe.com/reaction/1864518

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminoazetidine, 3-BOC protectedHCID 1519405—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantHCID 178461490HCID 178461490—
ProductHCID 60208257HCID 60208257—

Reaction Steps

1,1-dimethylethyl [1-((Z)-({3-[2-(4-fluorophenyl)ethyl]-4-oxo-3,4-dihydro-7-quinazolinyl}amino){[(1S,2S,3S,5R)-2,6,6-trimethylbicyclo[3.1.1 ]hept-3-yl]imino}methyl)-3-azetidinyl]carbamate (synthesized using 1,1-dimethylethyl 3-azetidinylcarbamate by the methods described previously) was treated with 4.0 N HCl/dioxane (4 mL) and stirred overnight. The reaction was then purified by preparatory HPLC to provide 3-amino-N-{3-[2-(4-fluorophenyl)ethyl]-4-oxo-3,4-dihydro-7-quinazolinyl}-N′-[(1S,2S,3S,5R)-2,6,6-trimethylbicyclo[3.1.1 ]hept-3-yl]-1-azetidinecarboximidamide as a white solid. LC/MS: M+H 517.20 at 2.19 minutes, Method D.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625909B2
Source datasetuspto-grants-2009_12
ORD IDord-13467d4616fa4591b9505e4f718250a8
Source noteuspto-grants-2009_12