methyl indoline-5-carboxylate Chemical Properties

Melting point:

67-69 °C

Boiling point:

331.0±31.0 °C(Predicted)

Density 

1.162±0.06 g/cm3(Predicted)

storage temp. 

Keep in dark place,Sealed in dry,2-8°C

solubility 

DMSO (Sparingly), Methanol (Slightly)

form 

Solid

pka

2.65±0.20(Predicted)

color 

Off-White

InChI

InChI=1S/C10H11NO2/c1-13-10(12)8-2-3-9-7(6-8)4-5-11-9/h2-3,6,11H,4-5H2,1H3

InChIKey

VVAPQJBMJBCZMH-UHFFFAOYSA-N

SMILES

N1C2=C(C=C(C(OC)=O)C=C2)CC1

Safety Information

HS Code 

2933998090

methyl indoline-5-carboxylate Usage And Synthesis

Synthesis

The general procedure for the synthesis of indoline-5-carboxylic acid methyl ester from indole-5-carboxylic acid was as follows: to a 10 mL solution of 1H-indole-5-carboxylic acid methyl ester (1 g, 5.71 mmol) in acetic acid was slowly added sodium cyano-borohydride (1.08 g, 17.18 mmol) at 0 °C, with the addition time being controlled to be within 5 minutes. The reaction mixture was stirred at room temperature for 1 hour. Upon completion of the reaction, water (3 mL) was added and all solvent was evaporated under reduced pressure. The residue was dissolved in ethyl acetate (150 mL) and saturated sodium bicarbonate solution (150 mL) for liquid-liquid separation. The aqueous phase was further extracted with ethyl acetate (3 x 75 mL). All organic phases were combined, washed with saturated saline (150 mL), dried over anhydrous sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The crude product was purified by fast column chromatography (eluent: 0-50% hexane solution of ethyl acetate containing 0.1% triethylamine) to afford the target product methyl indoline-5-carboxylate (0.99 g, 99% yield).

References

[1] Patent: WO2010/149685, 2010, A1. Location in patent: Page/Page column 51
[2] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 20, p. 5684 - 5688
[3] Patent: US2015/368195, 2015, A1. Location in patent: Paragraph 0072
[4] Organic and Biomolecular Chemistry, 2014, vol. 12, # 44, p. 8966 - 8976
[5] Journal of Medicinal Chemistry, 2006, vol. 49, # 14, p. 4425 - 4436

methyl indoline-5-carboxylate(141452-01-9)Related Product Information

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• 7-INDOLINECARBOXALDEHYDE
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• 6-Methoxycarbonyl-2,3-dihydro-1H-indole hydrochloride
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• INDOLE-5-METHANOL
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• METHYL OXINDOLE-7-CARBOXYLATE