HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372631Generated: November 1, 2026
Pyridine → Ethyl 3-chloro-4-(1-indolinylcarbonylamino)phenylacetate
https://huagongshe.com/reaction/1372631
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Indoline | HCID 10328 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | (4-Amino-3-chloro-phenyl)-acetic acid ethyl ester | HCID 17859298 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 3-chloro-4-(1-indolinylcarbonylamino)phenylacetate | HCID 17859294 | 274.2% |
Reaction Steps
In methylene chloride (50 ml), triphosgene (926 mg, 3.12 mmol) and then pyridine (5 ml) were added to ethyl 4-amino-3-chlorophenylacetate (2.00 g, 9.36 mmol) under stirring at 0° C. After stirring at the same temperature for 15 minutes, indoline (1.05 ml, 9.36 mmol) was added. The reaction mixture was further stirred for 15 minutes at room temperature. Water (50 ml) was added to the reaction mixture, followed by extraction with ethyl acetate (300 ml). The extract was washed with saturated brine, dried over anhydrous magnesium sulfate and distilled under reduced pressure to remove the solvent, whereby ethyl 3-chloro-4-(1-indolinylcarbonylamino)phenylacetate (3.07 g, 91%) was obtained as a pale pink crystalline powder.
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-c43f230416f64fb091f51102625deac3 |
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| Source note | uspto-grants-2007_01 |
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