HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389382Generated: October 31, 2026
Water → ethyl [4-({2-[5-(diphenylmethyl)-2-oxo-1(2H)-pyridinyl]ethyl}amino)-1H-indol-1-yl]acetate
https://huagongshe.com/reaction/2389382
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl 2-(4-amino-1h-indol-1-yl)acetate | HCID 16731708 | — |
| Reactant | 1-(2-chloroethyl)-5-(diphenylmethyl)-2(1H)-pyridinone | HCID 68538017 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl [4-({2-[5-(diphenylmethyl)-2-oxo-1(2H)-pyridinyl]ethyl}amino)-1H-indol-1-yl]acetate | HCID 59145309 | 41.2% |
Reaction Steps
To a stirring solution of ethyl (4-amino-1H-indol-1-yl)acetate (94 mg) in EtOH (7 mL) was added 1-(2-chloroethyl)-5-(diphenylmethyl)-2(1H)-pyridinone (70 mg) at ambient temperature. The reaction mixture was warmed to 50° C. After 24 hours, to the mixture was added water and the resulting mixture was extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous sodium sulfate and evaporated in vacuo. The residue was purified by preparative thin-layer chromatography (chloroform:EtOAc=5:1) to give ethyl [4-({2-[5-(diphenylmethyl)-2-oxo-1(2H)-pyridinyl]ethyl}amino)-1H-indol-1-yl]acetate (45 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273745B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-fea7ee1b709444c2844b8dad67d9095a |
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| Source note | uspto-grants-2012_09 |
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