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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657307Generated: November 1, 2026

Sodium Hydroxide → HCID 10419502, compound

https://huagongshe.com/reaction/1657307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-(1H-indol-2-yl)ethan-1-amineHCID 439752—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 10419502HCID 1041950251.6%

Reaction Steps

To a solution of 2-(indol-2-yl)ethylamine (2.7 g) in acetic acid (25 ml) at 15° C. wa added sodium cyanoborohydride (2.22 g) in one portion. The solution was stirred at room temperature for 15 hours and diluted with chilled water. The mixture was made basic with sodium hydroxide pellets and extracted three times with ether. The ether layer was washed with brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo to give 2-(2,3-dihydroindol-2-yl)ethylamine (1.41 g) as an oil. The oil was dissolved in tetrahydrofuran (50 ml) and treated with 1,1'-carbonyldiimidazole (1.13 g) at room temperature. The mixture was stirred at room temperature for 30 minutes. The reaction mixture was washed with brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. The residue was purified by silica gel column chromatography (30%-ethyl acetate-chloroform) to give crystals. The crystals were washed with ether to give 3,4,4a,5-tetrahydropyrimido[1,6-a]indol-1(2H)-one (0.74 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256780
Source datasetuspto-grants-1993_10
ORD IDord-861669ab33bd4834985795ecf6012334
Source noteuspto-grants-1993_10