HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290250Generated: October 26, 2026
Indole-3-Butyric Acid → HCID 18923893, compound
https://huagongshe.com/reaction/1290250
Participants
| Role | Name | HCID | Charge |
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| Reactant | Indole-3-Butyric Acid | HCID 8617 | — |
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | 2,3-Dihydro-7-hydroxy-1,4-benzodioxin-2-methanamine hydrochloride | HCID 18923890 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18923893 | HCID 18923893 | 17% |
Reaction Steps
3-Indolebutyric acid (1.0 g, 5.0 mmole), 1-hydroxybenzotriazole hydrate (0.8 g, 6.0 mmole) and 1,3-diisopropylcarbodiimide (1.9 ml, 12.0 mmole) were combined in 100 ml of DMF and stirred at room temperature for 2 hours under a nitrogen atmosphere. To this was added dropwise 7-hydroxy-2,3-dihydro-1,4-benzodioxin-2-methanamine hydrochloride (1.1 g, 5.0 mmole) in 50 ml of DMF and the mixture was further stirred for 24 hours. The solvent was removed and replaced with dichloromethane. The mixture was then washed with H2O. The separated organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuum. Chromatography on silica gel using first dichloromethane and then 2.5% methanol in dichloromethane as eluants gave 0.3 g (16%) of the desired product, (7-hydroxy-2,3-dihydro-benzo[1,4]dioxin-2-methyl)-4-(1H-indol-3-yl)-butanamide, as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05750724 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-11f8f38759314419b89248c522020b68 |
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| Source note | uspto-grants-1998_05 |
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