Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488472Generated: November 2, 2026

Ammonium Hydroxide → 11-(2-Benzyl-2,5-diazabicyclo(2.2.1) hept-5-yl)-dibenz[b,f][1,4]oxazepine

https://huagongshe.com/reaction/1488472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantO-(o-Aminophenoxy)benzoic acid lactamHCID 72374—
Reactant(1S,4S)-2-Benzyl-2,5-Diazabicyclo[2.2.1]heptaneHCID 14612543—
CatalystTitanium TetrachlorideHCID 24193—
SolventTolueneHCID 1140—
Product11-(2-Benzyl-2,5-diazabicyclo(2.2.1) hept-5-yl)-dibenz[b,f][1,4]oxazepineHCID 2209953149.1%

Reaction Steps

To a solution of 11-oxo-dibenz[b,f][1,4]oxazepine (Aldrich) (0.149 g, 0.0007 mol) in dry toluene (10 mL), was added (1S,4S)-2-benzyl-2,5-diazabicyclo(2.2.1)heptane (0.54 g, 0.003 mol) and TiCl4 (0.75 mL, 0.0008 mol) via syringe. The mixture was stirred at room temperature for 30 min then refluxed for 5 hrs. The reaction mixture was cooled and dumped into conc. NH4OH and extracted with CHCl3. The combined organic phases were dried (MgSO4) and concentrated in vacuo. The crude material was chromatographed (hexane:EtOAc, 1:1) to give 11-(2-benzyl-2,5-diazabicyclo(2.2.1) hept-5-yl)-dibenz[b,f][1,4]oxazepine (yield 0.131 g, mp 70°-72° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05674877
Source datasetuspto-grants-1997_10
ORD IDord-1ed58932397245018fc1e7032e4463b7
Source noteuspto-grants-1997_10