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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292772Generated: October 30, 2026

Sodium hydride → HCID 10573508, compound

https://huagongshe.com/reaction/2292772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantMethyl 5-bromovalerateHCID 79557—
ReactantHCID 10589888HCID 10589888—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 10573508HCID 10573508—

Reaction Steps

As described in Example 23, 125 mg (0.43 mmol) off 5-hydroxy-2-methyl-1-(phenylmethyl)-1H-indole-3-acetamide (Example 2), 30 mg of 60% NaH/mineral oil and 0.1 mL of 5-bromopentanoic acid methyl ester in 15 mL of DMSO were reacted to give 80 mg of 5-[[3-(2-amino-2-oxoethyl)-2-methyl-1-(phenylmethyl)-1H-indol-5-yl]oxy]pentanoic acid methyl ester, after chromatography on silica (eluted with CH2Cl2 →2% MeOH/CH2Cl2). This material in 5 mL of THF and 15 mL of EtOH was treated with 2 mL of 2N NaOH and the mixture stirred for 18 hours. After acidifying with 5N HCl, the mixture was extracted with EtOAc, the EtOAc solution washed with saturated NaCl solution, dried (Na2SO4), and concentrated at reduced pressure. The residue was dissolved in MeOH/CH2Cl2, concentrated and diluted with ether to give 80 mg (100% yield) of 5-[[3-(2-amino-2-oxoethyl)-2-methyl-1-(phenylmethyl)-1H-indol-5-yl]oxy]pentanoic acid, mp, 168°-169° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05684034
Source datasetuspto-grants-1997_11
ORD IDord-600f929fd7f1411a92e4633facda1d40
Source noteuspto-grants-1997_11