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62247-21-6

62247-21-6 Structure

62247-21-6 Structure
IdentificationMore
[Name]

(RS)-3-AMINO-3-(3-PYRIDYL)-PROPIONIC ACID
[CAS]

62247-21-6
[Synonyms]

3-AMINO-3-(3-PYRIDINYL)PROPANOIC ACID
3-AMINO-3-PYRIDIN-3-YLPROPANOIC ACID
3-AMINO-3-PYRIDIN-3-YL-PROPIONIC ACID
ART-CHEM-BB B013362
H-DL-PYG(3)-(C*CH2)OH
RARECHEM AK HC S246
(RS)-3-AMINO-3-(3-PYRIDYL)-PROPIONIC ACID
3-Amino-3-(3-pyridyl)propionic acid
[Molecular Formula]

C8H10N2O2
[MDL Number]

MFCD01549598
[Molecular Weight]

166.18
[MOL File]

62247-21-6.mol
Chemical PropertiesBack Directory
[Melting point ]

205.0 to 209.0 °C
[Boiling point ]

352.6±32.0 °C(Predicted)
[density ]

1.268±0.06 g/cm3(Predicted)
[storage temp. ]

-15°C
[Water Solubility ]

Slightly soluble in water
[form ]

powder to crystal
[pka]

3.06±0.12(Predicted)
[color ]

White to Almost white
[CAS DataBase Reference]

62247-21-6(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Hazard InformationBack Directory
[Chemical Properties]

White to light yellow powder
[Synthesis]

3-Pyridinecarboxaldehyde

500-22-1

(RS)-3-AMINO-3-(3-PYRIDYL)-PROPIONIC ACID

62247-21-6

Example 18 Synthesis of 3-amino-3-(3'-pyridinyl)propionic acid: ammonium acetate (194.28 g, 2.52 mol) was suspended in ethanol (285 g). A solution of pyridine-3-carboxaldehyde (62.9 g, 1.68 mol) in ethanol (80 g) was added dropwise to the suspension over a period of 10 min at 15°C to 20°C. The reaction was carried out by stirring the mixture for 1 h until the reaction was completed. The reaction mixture was stirred for 1 hour until a pale yellow clarified solution was formed. Subsequently, an ethanol (235 g) suspension of malonic acid (174.86 g, 1.68 mol) was added over 30 minutes. After stirring at room temperature for 30 min, the reaction mixture was heated to reflux (78°C) and maintained for 5 hours. Gas release was observed during the reaction. after 3 to 4 hours, a white solid began to precipitate. The orange suspension was cooled to 15°C to 20°C to form a thick slurry. Methanol (80 g) was added to the slurry and the reaction mixture was heated to reflux (65°C) again. The suspension was thermally filtered and the filter cake was washed with three parts of hot methanol (120 g, 55°C to 65°C). The wet product was dried under vacuum at 70°C to 80°C to give a colorless solid product (137.73 g, 49.3% yield). the LC purity was 95.8%.

[References]

[1] Patent: US2002/68829, 2002, A1
[2] Patent: US2002/68829, 2002, A1
[3] Patent: US5602155, 1997, A
[4] Patent: US5681820, 1997, A
[5] Patent: US5639765, 1997, A
Spectrum DetailBack Directory
[Spectrum Detail]

(RS)-3-AMINO-3-(3-PYRIDYL)-PROPIONIC ACID(62247-21-6)1HNMR
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