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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895023Generated: October 26, 2026

Tetramethylammonium fluoride → 2-propyl-2-(1H-pyrrolo[2,3-b]pyridine-5-carbonyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1895023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetramethylammonium fluorideHCID 67803—
Reactant2-propyl-2-(1-triisopropylsilanyl-1H-pyrrolo[2,3-b]pyridine-5-carbonyl)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 66687476—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
Product2-propyl-2-(1H-pyrrolo[2,3-b]pyridine-5-carbonyl)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 6668838586%

Reaction Steps

To a stirred solution of 2-propyl-2-(1-triisopropylsilanyl-1H-pyrrolo[2,3-b]pyridine-5-carbonyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (0.415 g, 0.809 mmol) in THF (7.5 mL) at ambient temperature under nitrogen was added TMAF (0.753 g, 8.09 mmol). The reaction mixture was stirred for one hour, then diluted with saturated aqueous NaHCO3 (30 mL) and water (15 mL) and extracted with EtOAc. The combined organic extracts were washed with brine, dried (MgSO4), filtered, and concentrated in vacuo to a pale yellow gum. Purification by chromatography (silica, 50 to 100% EtOAc in hexanes) gave 2-propyl-2-(1H-pyrrolo[2,3-b]pyridine-5-carbonyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (0.247 g, 0.692 mmol, 86%) as a colourless foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513425B2
Source datasetuspto-grants-2013_08
ORD IDord-0a4080911e844729b21274d2af0ac3fc
Source noteuspto-grants-2013_08