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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069582Generated: October 29, 2026

Sodium hydride → 4-(1-Benzyl-3-carbamoylmethyl-2-methyl-1H-indol-6-yloxy)-butyric acid ethyl ester

https://huagongshe.com/reaction/1069582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl 4-bromobutyrateHCID 76300—
Reactant6-hydroxy-2-methyl-1-(phenylmethyl)-1H-indole-3-acetamideHCID 10565732—
ReactantHexane methylene chloride methanolHCID 21959077—
SolventWaterHCID 962—
Product4-(1-Benzyl-3-carbamoylmethyl-2-methyl-1H-indol-6-yloxy)-butyric acid ethyl esterHCID 1057350976%

Reaction Steps

A solution of 294 mg (1 mmol) of 6-hydroxy-2-methyl-1-(phenylmethyl)-1H-indole-3-acetamide was treated with 40 mg (1 mmol) of 60% NaH/mineral oil and after 1 hours, 0.15 mL (1 mmol) of ethyl 4-bromobutyrate was added. The mixture was stirred for 2 hours, diluted with water and extracted with EtOAc. The EtOAc solution was washed with NaCl solution, dried (MgSO4), and concentrated at reduced pressure. The residue was chromatographed on silica eluting with EtOAc to give (after crystallizing from CH2Cl2/MeOH/hexane, 228 mg (76% yield) of 4-[[3-(2-amino-2-oxoethyl)-2-methyl-1-(phenylmethyl)-1H-indol-6-yl]oxy]butanoic acid ethyl ester, mp, 126-133° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06252084B1
Source datasetuspto-grants-2001_06
ORD IDord-b0822de911be4d3e926d6fc04d5bdc5f
Source noteuspto-grants-2001_06