HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055548Generated: November 1, 2026
Diisopropylethylamine → HCID 59657535, compound
https://huagongshe.com/reaction/2055548
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | 3H-spiro[2-benzofuran-1,4'-piperidine] | HCID 10442498 | — |
| Reactant | 6-Chloro-2-methyl-1H-indole-3-carboxylic acid | HCID 45121065 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59657535 | HCID 59657535 | 49.7% |
Reaction Steps
To a solution of 0.040 g (0.19 mmol) 6-chloro-2-methyl-1H-indole-3-carboxylic acid, 0.069 ml (0.40 mmol) N,N-diisopropylethylamine and 0.061 g (0.19 mmol) 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate in 1 ml dry N,N-dimethylformamide were added 0.036 g (0.19 mmol) spiro[isobenzofuran-1(3H), 4′-piperidine] at room temperature. After stirring for 1 h the reaction mixture was quenched with 0.5 M aqueous sodium hydroxide solution (20 ml) and extracted with ethyl acetate (2×30 ml). The combined organic layers were washed with water (2×30 ml) and brine (1×30 ml), dried over sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography (n-heptane/ethyl acetate) to give the title compound (0.036 g, 49%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07332501B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-6525a800472c43e096e2ab6479552074 |
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| Source note | uspto-grants-2008_02 |
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