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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-Benzyloxy-4-methoxymethyl-beta-carboline-3-carbaldehyde Oxime | HCID 136364613 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 6-Benzyloxy-3-(3-isoxazolyl)-4-methoxymethyl-beta-carboline | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04933345 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-ef98fcb174f54bd8904265fa58ff64db |
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| Source note | uspto-grants-1990_06 |
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