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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753021Generated: October 29, 2026

(4-Chlorophenyl)acetic acid → N-(5-{1-[2-(tert-Butyl-dimethyl-silanyloxy)-1,1-dimethyl-ethyl]-7-fluoro-1H-pyrrolo[3,2-c]pyridine-3-carbonyl}-pyridin-3-yl)-2-(4-chloro-phenyl)-acetamide

https://huagongshe.com/reaction/1753021

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Chlorophenyl)acetic acidHCID 15880—
ReactantDiisopropylethylamineHCID 81531—
ReactantPropylphosphonic anhydrideHCID 111923—
ReactantHCID 90092825HCID 90092825—
SolventTetrahydrofuranHCID 8028—
ProductN-(5-{1-[2-(tert-Butyl-dimethyl-silanyloxy)-1,1-dimethyl-ethyl]-7-fluoro-1H-pyrrolo[3,2-c]pyridine-3-carbonyl}-pyridin-3-yl)-2-(4-chloro-phenyl)-acetamideHCID 90093312—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of (5-amino-pyridin-3-yl)-{1-[2-(tert-butyl-dimethyl-silanyloxy)-1,1-dimethyl-ethyl]-7-fluoro-1H-pyrrolo[3,2-c]pyridin-3-yl}-methanone (Preparation 29, 35 mg, 70 μmol), (4-chloro-phenyl)-acetic acid (13 mg, 79 μmol) and DIPEA (31 μL, 237 μmol) in THF (3 mL), T3P (151 μL, 237 μmol) was added and the mixture stirred at 25° C. for 18 hours. The reaction was evaporated under reduced pressure, the residue partitioned between water and ethyl acetate, the organic extracts washed with saturated sodium bicarbonate solution, dried over sodium sulphate, evaporated in vacuo and triturated with pentane-ether to afford the title compound as an off white solid (74%, 35 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163021B2
Source datasetuspto-grants-2015_10
ORD IDord-6b24718022fc44a896a90a4495a708b4
Source noteuspto-grants-2015_10