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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845329Generated: October 30, 2026

Dicyclohexylcarbodiimide → HCID 15612344, compound

https://huagongshe.com/reaction/845329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactanttert-Butylacetic acidHCID 14057—
Reactant(+/-)-alpha-amino-alpha-methyl-N-(2-phenylethyl)-1H-indole-3-propanamideHCID 14560809—
ReactantHydroxybenzothiazole hydrateHCID 178526942—
SolventEthyl AcetateHCID 8857—
ProductHCID 15612344HCID 1561234422.6%

Reaction Steps

A solution of 0.14 g (1.2 mmol) of tert-butylacetic acid in 5 ml of ethyl acetate was treated with 0.367 g (2.4 mmol) of hydroxybenzothiazole hydrate, and 0.247 g (1.2 mmol) of dicyclohexylcarbodiimide. After stirring at room temperature for one hour, the product of Example 12 (0.321 g, 1 mmol) was added, together with a few additional milliliters of ethyl acetate. This mixture was stirred overnight at room temperature, and the crude product isolated. Following purification by column chromatography on silica gel, there was obtained 0.095 g of (±)-α-[(2,3-dimethyl-1-oxobutyl)-amino ]-α-methyl-N-(2-phenylethyl)-1H-indole-3-propanamide, mp 104°-109° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04757151
Source datasetuspto-grants-1988_07
ORD IDord-5f11e31640b6411aa61075715cdf0dea
Source noteuspto-grants-1988_07