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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440431Generated: October 29, 2026

Water → N-(3-Fluoro-4-pyridinyl)-N-(3-methyl-1H-indol-1-yl)glycine ethyl ester

https://huagongshe.com/reaction/440431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl chloroacetateHCID 7751—
ReactantSodium hydrideHCID 24758—
ReactantN-(3-Fluoro-4-pyridinyl)-3-methyl-1H-indol-1-amineHCID 9942843—
SolventDimethylformamideHCID 6228—
ProductN-(3-Fluoro-4-pyridinyl)-N-(3-methyl-1H-indol-1-yl)glycine ethyl esterHCID 15818612—

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a suspension of NaH (60% in oil, 1.48 g) in 10 ml of dimethylformamide (DMF) at ice bath temperature was added dropwise a solution of N-(3-fluoro-4-pyridinyl)-3-methyl-1H-indol-1-amine (8.5 g) in 40 ml of DMF. when addition was complete, the mixture was stirred for 15 minutes at ice bath temperature, and then cooled to -20° C. Ethyl chloroacetate (3.95 ml) was added dropwise in 10 ml of DMF. The mixture was stirred at -20° C. for one hour. The mixture was then poured into water and extracted with ethyl acetate. The organic layer was washed with water and dried (sat. NaCl, anhy. MgSO4). After filtering, the solvent was evaporated to yield an oil (12.2 g) which was eluted with 10% ethyl acetate/DCM on a silica gel column via HPLC. The desired fractions were evaporated to yield 6.9 g of a solid, m.p. 105°-108° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05519131
Source datasetuspto-grants-1996_05
ORD IDord-cfc0b6b532734aa9b257e44ebadd2bab
Source noteuspto-grants-1996_05