Pyrrolo[1,2-a]pyrazine, 1,2,3,4-tetrahydro- (9CI)

Pyrrolo[1,2-a]pyrazine, 1,2,3,4-tetrahydro- (9CI) Suppliers list
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CAS:71257-38-0
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CAS:71257-38-0
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Pyrrolo[1,2-a]pyrazine, 1,2,3,4-tetrahydro- (9CI) manufacturers

Pyrrolo[1,2-a]pyrazine, 1,2,3,4-tetrahydro- (9CI) Basic information
Product Name:Pyrrolo[1,2-a]pyrazine, 1,2,3,4-tetrahydro- (9CI)
Synonyms:Pyrrolo[1,2-a]pyrazine, 1,2,3,4-tetrahydro- (9CI);pyrrolo[1,2-a]pyrazine, 1,2,3,4-tetrahydro-;Albb-009270;1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine(SALTDATA: FREE);1H,2H,3H,4H-pyrrolo[1,2-a]pyrazine;1,2,3,4-TETRAHYDROPYRROLO[1,2-A]PYRAZINE 2-BUTENEDIOATE
CAS:71257-38-0
MF:C7H10N2
MW:122.17
EINECS:
Product Categories:AMINETERTIARY
Mol File:71257-38-0.mol
Pyrrolo[1,2-a]pyrazine, 1,2,3,4-tetrahydro- (9CI) Structure
Pyrrolo[1,2-a]pyrazine, 1,2,3,4-tetrahydro- (9CI) Chemical Properties
Boiling point 239.6±28.0 °C(Predicted)
density 1.18±0.1 g/cm3(Predicted)
storage temp. 2-8°C(protect from light)
pka7.40±0.20(Predicted)
AppearanceColorless to light yellow Liquid
Safety Information
RIDADR 3265
HazardClass IRRITANT
PackingGroup 
HS Code 2933998090
MSDS Information
Pyrrolo[1,2-a]pyrazine, 1,2,3,4-tetrahydro- (9CI) Usage And Synthesis
Synthesis
2-(1H-PYRROL-1-YL)-1-ETHANAMINE

29709-35-1

Formaldehyde

50-00-0

Pyrrolo[1,2-a]pyrazine, 1,2,3,4-tetrahydro- (9CI)

71257-38-0

General procedure for the synthesis of 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine from 2-(1H-pyrrol-1-yl)ethylamine and formaldehyde: 2-(1H-pyrrol-1-yl)ethylamine (2 g, 18 mmol) was dissolved in 40 mL of ethanol, followed by the addition of 40% aqueous formaldehyde (1.5 mL, 18 mmol) and the slow dropwise addition of 1 mL trifluoroacetic acid. The reaction mixture was heated to 50 °C and maintained for 15 minutes, then cooled to room temperature and stirred continuously for 12 hours. Upon completion of the reaction, the solvent was removed by concentration under reduced pressure, diluted by adding 50 mL of ethyl acetate, and the organic phase was washed with 50 mL of saturated sodium bicarbonate solution, followed by drying with anhydrous sodium sulfate and filtration. Finally, the filtrate was concentrated by decompression to afford 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine (1.60 g, 72.7% yield) as a light yellow oil.

References[1] Patent: EP2604610, 2013, A1. Location in patent: Paragraph 0082; 0084
[2] Patent: US2013/131068, 2013, A1. Location in patent: Paragraph 0105
[3] Patent: US2008/153843, 2008, A1. Location in patent: Page/Page column 75
[4] Patent: CN108250128, 2018, A. Location in patent: Paragraph 0787; 0789; 0792; 0793
[5] Patent: US2009/186899, 2009, A1. Location in patent: Page/Page column 37; 41
Tag:Pyrrolo[1,2-a]pyrazine, 1,2,3,4-tetrahydro- (9CI)(71257-38-0) Related Product Information
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