| Identification | Back Directory | [Name]
METHYL N-BENZYL-3-PYRROLIDINECARBOXYLATE | [CAS]
17012-21-4 | [Synonyms]
Methyl 1-benzyllpyrrolidi...
METHYL 1-BENZYLPYRROLIDINE-3-CARBOXYLATE
METHYL N-BENZYL-3-PYRROLIDINECARBOXYLATE
Methyl 1-benzyl-3-pyrrolidinecarboxylate
Methyl 1-benzyllpyrrolidine-3-carboxylate
MethylN-benzylpyrrolidine-3-carboxylate,97%
Methyl 1-benzylpyrrolidine-3-carboxylate 97%
Methyl N-benzylpyrrolidine-3-carboxylate, 97%
1-Benzyl-3-pyrrolidinecarboxylic acid methyl ester
1-BENZYL-PYRROLIDINE-3-CARBOXYLIC ACID METHYL ESTER
3-Pyrrolidinecarboxylic acid, 1-(phenylMethyl)-, Methyl ester
1-Benzyl-3-(methoxycarbonyl)pyrrolidine, Methyl 1-(phenylmethyl)pyrrolidine-3-carboxylate | [Molecular Formula]
C13H17NO2 | [MDL Number]
MFCD04038678 | [MOL File]
17012-21-4.mol | [Molecular Weight]
219.28 |
| Chemical Properties | Back Directory | [Boiling point ]
98℃/0.2mm | [density ]
1.08 | [refractive index ]
1.5211 | [storage temp. ]
Sealed in dry,2-8°C | [form ]
clear liquid | [pka]
8.34±0.40(Predicted) | [color ]
Colorless to Light orange to Yellow | [Water Solubility ]
Sparingly soluble in water.(0.26 g/L) (25°C), | [InChI]
InChI=1S/C13H17NO2/c1-16-13(15)12-7-8-14(10-12)9-11-5-3-2-4-6-11/h2-6,12H,7-10H2,1H3 | [InChIKey]
GDWFCUOFVSNTTG-UHFFFAOYSA-N | [SMILES]
N1(CC2=CC=CC=C2)CCC(C(OC)=O)C1 | [CAS DataBase Reference]
17012-21-4 |
| Hazard Information | Back Directory | [Uses]
It is used as pharmaceutical intermediate. Benzoylthiophenes are allosteric enhancers (AE) of agonist activity at the A1 adenosine receptor. | [Synthesis Reference(s)]
The Journal of Organic Chemistry, 33, p. 3637, 1968 DOI: 10.1021/jo01273a063 | [Synthesis]
A trifluoroacetic acid solution of 44.0 g (0.4 mol) at a mass concentration of 10% was prepared by adding 1530.0 g (6.5 mol) of N-(methoxymethyl)-N-(trimethylsilylmethyl)benzylamine, 31.80 g (3.7 mol) of methyl acrylate, and 38 mL of dichloromethane to a 250 mL multi-neck reaction flask. The trifluoroacetic acid solution was added slowly dropwise at 0 °C, and after completion of the dropwise addition, the reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the mixture was concentrated under reduced pressure and the residue was washed sequentially with saturated sodium bicarbonate solution and saturated sodium chloride solution. The organic phases were combined, dried with anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to give 1420.0 g of 1-benzylpyrrolidine-3-carboxylic acid methyl ester crude product in 100% yield. | [References]
[1] Bioorganic and Medicinal Chemistry Letters, 2004, vol. 14, # 19, p. 4861 - 4866
[2] Organic Process Research and Development, 2009, vol. 13, # 2, p. 292 - 296
[3] Synthesis, 2006, # 16, p. 2646 - 2648
[4] Synlett, 2015, vol. 26, # 13, p. 1815 - 1818
[5] Chemical & Pharmaceutical Bulletin, 1985, vol. 33, # 7, p. 2762 - 2766 |
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