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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107054Generated: November 3, 2026

Sodium Hydroxide → 6-Benzyloxy-3-(3-isoxazolyl)-4-methoxymethyl-beta-carboline

https://huagongshe.com/reaction/2107054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantN-bromobutanimideHCID 67184—
Reactant6-Benzyloxy-4-methoxymethyl-beta-carboline-3-carbaldehyde OximeHCID 136364613—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product6-Benzyloxy-3-(3-isoxazolyl)-4-methoxymethyl-beta-carbolineHCID 14372936—

Reaction Steps

0.55 g (1.5 mmol) of 6-benzyloxy-4-methoxymethyl-β-carboline-3-carbaldehyde oxime is dissolved in 30 ml of dry DMF and combined with 0.3 g (1.7 mmol) of N-bromosuccinimide (dissolved in 5 ml of DMF). The reaction mixture is stirred for 10 minutes at room temperature and then 1.5 eq. of trimethylsilylacetylene and 1 ml of triethylamine are added. After 4 hours of agitation at room temperature, 5 ml of 1-molar sodium hydroxide solution is added and subsequently agitation is continued for another hour. The solution is poured into ice water and extracted with ethyl acetate. The organic phase is dried over magnesium sulfate and the solvent drawn off. The resultant product is purified by column chromatography on silica gel with ethyl acetate as the eluent. Melting point: 123°-126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04933345
Source datasetuspto-grants-1990_06
ORD IDord-ef98fcb174f54bd8904265fa58ff64db
Source noteuspto-grants-1990_06