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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976697Generated: November 1, 2026

Sodium Carbonate → methyl (S)-2-[3-(2-benzyloxy-1-methylethyl)-2-triethylsilyl-1H-pyrrolo[2,3-b]pyridin-5-yl]-2-methylpropanoate

https://huagongshe.com/reaction/1976697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(S)-(4-benzyloxy-3-methylbut-1-ynyl)triethylsilaneHCID 11323707—
ReactantMethyl 2-(6-amino-5-iodopyridin-3-yl)-2-methylpropanoateHCID 15887215—
CatalystHCID 178418807HCID 178418807—
SolventDimethylformamideHCID 6228—
Productmethyl (S)-2-[3-(2-benzyloxy-1-methylethyl)-2-triethylsilyl-1H-pyrrolo[2,3-b]pyridin-5-yl]-2-methylpropanoateHCID 1588721688.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

A vigorously stirred suspension of methyl 2-(6-amino-5-iodopyridin-3-yl)-2-methylpropanoate (4.61 g, 14.4 mmol), (S)-(4-benzyloxy-3-methylbut-1-ynyl)triethylsilane (4.98 g, 17.3 mmol), Pd(dppf)Cl2·CH2Cl2 (0.59 g, 0.72 mmol) LiCl (0.61 g, 14.4 mmol), Na2CO3 (3.82 g, 36.0 mmol) and N,N-dimethylformamide (60 mL) was degassed via three vacuum/nitrogen ingress cycles and the resulting mixture was heated at approximately 90° C. overnight. After cooling to ambient temperature, the reaction mixture was diluted with ethyl acetate and filtered through celites washing copiously with ethyl acetate. The filtrate was poured into water and extracted with ethyl acetate (x3). The combined organic extract was washed with brine, dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (gradient elution; 20-25% ethyl acetate/hexanes as eluent) to give the title compound as a viscous oil (6.11 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06228867B1
Source datasetuspto-grants-2001_05
ORD IDord-e29b8654a1e94df6acf6d1750539a258
Source noteuspto-grants-2001_05