HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170859Generated: October 27, 2026
1H-Indole-5-Carboxylic Acid → HCID 67168639, compound
https://huagongshe.com/reaction/2170859
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1H-Indole-5-Carboxylic Acid | HCID 74280 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | 4-(4-Chlorophenoxy)piperidine hydrochloride | HCID 17749791 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67168639 | HCID 67168639 | 94% |
Reaction Steps
To a stirred solution of 4-(4-chlorophenoxy)piperidine hydrochloride (300 mg, 1.21 mmol), 1H-indole-5-carboxylic acid (195 mg, 1.21 mmol), and N,N-diisopropylethylamine (0.85 mL, 4.84 mmol) in N,N-dimethylformamide (10 mL) was add HBTU (688 mg, 1.81 mmol) at room temperature. After stirring at 60° C. for 2 hours, the mixture was poured into water (50 mL). This was extracted with ethyl acetate (50 mL) and washed with water (50 mL). The organic layer was dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica-gel column chromatography (NH-gel, eluting with n-hexane/ethyl acetate=1/1) to give 403 mg (94% yield) of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051296B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-5a3196fa23304d54ad69491addb8b8f3 |
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| Source note | uspto-grants-2015_06 |
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