3-Benzyl-3,7-diazabicyclo[3.3.0]octane

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CAS:86732-22-1
Purity:99% Package:1kg;1USD
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CAS:86732-22-1
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CAS:86732-22-1
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CAS:86732-22-1
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3-Benzyl-3,7-diazabicyclo[3.3.0]octane manufacturers

3-Benzyl-3,7-diazabicyclo[3.3.0]octane Basic information
Product Name:3-Benzyl-3,7-diazabicyclo[3.3.0]octane
Synonyms:2-Benzyl-Octahydro-Pyrrolo[3,4-C]Pyrrole HCl;3-Benzyl-3,7-diazabicyclo[3.3.0]octane;3-BENZYL-3,7-DIAZABICYCLO[3.3.0]OCTANE,98%;4,5-DIHYDROBENZO[D...;Octahydro-2-benzylpyrrolo[3,4-c]pyrrole;Pyrrolo[3,4-c]pyrrole, octahydro-2-(phenylmethyl)-;2-BENZYL-OCTAHYDRO-PYRROLO [3,4-C] PYRROLE;5-(phenylmethyl)-2,3,3a,4,6,6a-hexahydro-1H-pyrrolo[3,4-c]pyrrole
CAS:86732-22-1
MF:C13H18N2
MW:202.3
EINECS:
Product Categories:Heterocycles series;Amines and Anilines
Mol File:86732-22-1.mol
3-Benzyl-3,7-diazabicyclo[3.3.0]octane Structure
3-Benzyl-3,7-diazabicyclo[3.3.0]octane Chemical Properties
storage temp. Keep in dark place,Inert atmosphere,Room temperature
AppearanceColorless to light yellow Liquid
Safety Information
Hazard Codes Xn
Risk Statements 22
HS Code 2933998090
MSDS Information
3-Benzyl-3,7-diazabicyclo[3.3.0]octane Usage And Synthesis
Synthesis
5-BENZYL-TETRAHYDROPYRROLO[3,4-C]PYRROLE-1,3(2H,3AH)-DIONE

848591-86-6

3-Benzyl-3,7-diazabicyclo[3.3.0]octane

86732-22-1

The general procedure for the synthesis of 3-benzyl-3,7-diazabicyclo[3.3.0]octane from the compound (CAS:848591-86-6) was as follows: first, 5-benzyltetrahydropyrrolo[3,4-c]pyrrole-1,3-dione (4.9 g, 0.021 mol) was dissolved in pre-cooled to 0 °C anhydrous tetrahydrofuran (THF) under nitrogen protection ( 50 mL). Subsequently, a THF solution of lithium aluminum hydride (63 mL, 1 M, 0.063 mol) was slowly added dropwise over 30 min while keeping the reaction mixture at 0 °C. After the dropwise addition was completed, the reaction mixture was stirred at room temperature for 30 minutes and then heated to reflux for 4 hours. Upon completion of the reaction, the mixture was cooled to 0 °C and the reaction was quenched by slow addition of excess sodium sulfate decahydrate solid. The mixture was returned to room temperature and stirring was continued for 16 hours. The solid was removed by filtration and the filtrate was washed with ethyl acetate (3 x 100 mL). The filtrates were combined and concentrated to give 4.2 g (99% yield) of the waxy solid product, which was analyzed by mass spectrometry to show m/z 203 (M + H).

References[1] Patent: WO2008/57938, 2008, A1. Location in patent: Page/Page column 30
[2] Patent: WO2006/12396, 2006, A1. Location in patent: Page/Page column 21; 34
[3] Patent: WO2013/71697, 2013, A1. Location in patent: Paragraph 00248
[4] Patent: US2014/228361, 2014, A1. Location in patent: Paragraph 0368-0369
[5] Patent: US2005/101602, 2005, A1. Location in patent: Page/Page column 28
3-Benzyl-3,7-diazabicyclo[3.3.0]octane Preparation Products And Raw materials
Raw materials5-BENZYL-TETRAHYDROPYRROLO[3,4-C]PYRROLE-1,3(2H,3AH)-DIONE-->2-BENZYL-TETRAHYDROPYRROLO[3,4-C] PYRROLE-1,3(2H,3AH)-DIONE-->Tetrahydrofuran-->Sodium sulfate-->Lithium Aluminum Hydride-->Water
Preparation ProductsJNJ-42847922
Tag:3-Benzyl-3,7-diazabicyclo[3.3.0]octane(86732-22-1) Related Product Information
Benzyl alcohol Benzyl chloride Benzyl benzoate Pyrrole 3-METHYLADENINE Benzyl acetate 2,5-Dibenzyltetrahydropyrrolo[3,4-c]pyrrole-1,3-dione Benzyl CIS-5-BENZYL-2-BOC-HEXAHYDROPYRROLO[3,4-C]PYRROLE CIS-5-BENZYLTETRAHYDROPYRROLO[3,4-C]PYRROLE-1,3(2H,3AH)-DIONE 2-BENZYL-TETRAHYDROPYRROLO[3,4-C] PYRROLE-1,3(2H,3AH)-DIONE METHYL 2-(5-BENZYL-4,6-DIOXO-3-PHENYLOCTAHYDROPYRROLO[3,4-C]PYRROL-1-YL)ACETATE 3-Benzyl-3,7-diazabicyclo[3.3.0]octane 2-BENZYL-OCTAHYDRO-PYRROLO[3,4-C]PYRROLE HYDROCHLORIDE CBI-BB ZERO/005082 5-benzyl-1-(5-methyl-2-furyl)octahydropyrrolo[3,4-c]pyrrole cis-2-Benzyloctahydropyrrolo[3,4-c]pyrrole METHYL 1,5-DIBENZYL-3-(4-CHLOROPHENYL)-4,6-DIOXOOCTAHYDROPYRROLO[3,4-C]PYRROLE-1-CARBOXYLATE