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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198968Generated: October 31, 2026

Ethyl 3-(triphenyl-lambda~5~-phosphanylidene)propanoate → t-butyl 4-[6-(N-cyclopentylmethylcarbamoyl)-3-(2-ethoxycarbonyl-1-propenyl)indol-1-ylmethyl]-3-methoxybenzoate

https://huagongshe.com/reaction/1198968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(triphenyl-lambda~5~-phosphanylidene)propanoateHCID 12607919—
Reactantt-butyl 4-[6-(N-cyclopentylmethylcarbamoyl)-3-formylindol-1-ylmethyl]3-methoxybenzoateHCID 15013776—
Solvent1,4-DioxaneHCID 31275—
Productt-butyl 4-[6-(N-cyclopentylmethylcarbamoyl)-3-(2-ethoxycarbonyl-1-propenyl)indol-1-ylmethyl]-3-methoxybenzoateHCID 53856301100.6%

Reaction Steps

A solution of t-butyl 4-[6-(N-cyclopentylmethylcarbamoyl)-3-formylindol-1-ylmethyl]3-methoxybenzoate (Example 1, part(f)) (2.8 g) and (carbethoxyethylidene)triphenylphosphorane (4.6 g) in dioxane (29 ml) was heated at reflux for 18 hours. The solvent was evaporated. The resultant residue was purified by flash chromatography on silica gel (192 ml), eluting with 1:4 ethyl acetate:hexane to give t-butyl 4-[6-(N-cyclopentylmethylcarbamoyl)-3-(2-ethoxycarbonyl-1-propenyl)indol-1-ylmethyl]-3-methoxybenzoate (3.3 g, 100%) as a light yellow solid; mp 118°-120°; NMR (80 MHz, CDCl3) 2.15(d, 3H, CCH3), 3.40(dd, 2H, NHCH2), 5.42(s, 2H, NCH2), 6.22(br t, 1H, NH), 6.78(d, 1H, Ar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04898863
Source datasetuspto-grants-1990_02
ORD IDord-2bc86316e88e4a7b8a84a7484aef4554
Source noteuspto-grants-1990_02