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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428504Generated: October 31, 2026

Iodobenzene → HCID 57459621, compound

https://huagongshe.com/reaction/1428504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodobenzeneHCID 11575—
Reactanttert-Butyl 4,7-diazaspiro[2.5]octane-7-carboxylateHCID 46942212—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 57459621HCID 57459621—

Reaction Conditions

Temperature120 °C

Reaction Steps

A stirred solution of 4,7-diaza-spiro[2.5]octane-7-carboxylic acid tert-butyl ester (0.1 g, 0.471 mmol) [C.A.S. 886766-28-5], iodobenzene (0.026 ml, 0.236) and CsOH (0.079 g, 0.471 mmol) in DMSO (1 ml) was heated in a sealed tube at 120° C. for 20 min. After cooling, additional 4,7-diaza-spiro[2.5]octane-7-carboxylic acid tert-butyl ester (2 eq.) was added, and the mixture was then heated at 120° C. for 20 min. The mixture was cooled. The mixture was washed with NH4Cl (aqueous sat. solution) was added and extracted with Et2O. The organic phase was separated, washed with water, dried (Na2SO4) and concentrated in vacuo. The crude product was purified by manifold (Sep-Pak® silica cartridge; DCM as eluent). The desired fractions were collected and concentrated in vacuo to yield intermediate D61 (0.021 g, 31%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937060B2
Source datasetuspto-grants-2015_01
ORD IDord-56289854288d40d1ac66a712e4eaa1e6
Source noteuspto-grants-2015_01