HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372599Generated: October 26, 2026
Triethylamine → Ethyl 3-chloro-4-(3-indolylcarbonylamino)phenylacetate
https://huagongshe.com/reaction/1372599
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Indole-3-Carboxylic Acid | HCID 69867 | — |
| Reactant | (4-Amino-3-chloro-phenyl)-acetic acid ethyl ester | HCID 17859298 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 3-chloro-4-(3-indolylcarbonylamino)phenylacetate | HCID 17858762 | 56.4% |
Reaction Steps
EDC•HCL (1.78 g, 9.28 mmol) was added to a solution of indole-3-carboxylic acid (1.00 g, 6.21 mmol), ethyl 4-amino-3-chlorophenylacetate (1.33 g, 6.22 mmol) and triethylamine (1.80 mL, 12.9 mmol). The mixture was stirred at 70° C. for 24 hours. After cooling to room temperature, the reaction mixture was added with water (30 ml), followed by extraction with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from hexane-ethyl acetate (1:1, v/v) eluate fractions, ethyl 3-chloro-4-(3-indolylcarbonylamino)phenylacetate (1.25 g, 56%) was obtained as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157487B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-49eed944d4ce442b9151eecd8c02f343 |
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| Source note | uspto-grants-2007_01 |
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