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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500504Generated: October 27, 2026

Triethylamine → tert-Butyl 2-{7-[3-(4-cyanoanilino)propyl]-9-oxa-3,7-diazabicyclo[3.3.1]non-3-yl}ethylcarbamate

https://huagongshe.com/reaction/500504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl N-(2-bromoethyl)carbamateHCID 4103526—
Reactant4-{[3-(9-Oxa-3,7-diazabicyclo[3.3.1]non-3-yl)propyl]amino}benzonitrileHCID 18540385—
SolventDimethylformamideHCID 6228—
ProductAmmonium HydroxideHCID 14923—
Producttert-Butyl 2-{7-[3-(4-cyanoanilino)propyl]-9-oxa-3,7-diazabicyclo[3.3.1]non-3-yl}ethylcarbamateHCID 988888491.9%

Reaction Conditions

Temperature35 °C

Reaction Steps

To a solution of tert-butyl 2-bromoethylcarbamate (4.21 g, 0.019 mol; see Preparation R above) in DMF (65 mL) was added 4-{[3-(9-oxa-3,7-diazabicyclo[3.3.1]non-3-yl)propyl]amino}benzonitrile (see Preparation C above, 4.48 g, 0.016 mol) and triethylamine (3.27 mL, 0.024 mol). The mixture was stirred overnight at 35° C. and then concentrated in vacuo. The residue was dissolved in dichloromethane (80 mL) and washed with saturated sodium chloride. The aqueous layer was extracted with dichloromethane (1×150 mL). The combined organic extracts were dried (Na2SO4) and concentrated in vacuo. The crude red-brown oil was chromatographed (×2) on silica gel eluting with chloroform:methanol:conc. NH4OH (9:1:0.02) to afford 3.75 g (56%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772229B2
Source datasetuspto-grants-2010_08
ORD IDord-1b51881f0a3e4ff793c665f0c0fa0d79
Source noteuspto-grants-2010_08