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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182389Generated: November 2, 2026

Triethylamine → benzyl (2S)-1-{(2S)-2-[(tert-butoxycarbonyl)amino]propionyl}-2,3-dihydro-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1182389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTert-butoxycarbonylalanineHCID 85082—
Reactantbenzyl 2,3-dihydro-1H-indole-2-carboxylate para-toluenesulphonateHCID 86612765—
SolventEthyl AcetateHCID 8857—
Productbenzyl (2S)-1-{(2S)-2-[(tert-butoxycarbonyl)amino]propionyl}-2,3-dihydro-1H-indole-2-carboxylateHCID 86612047—

Reaction Conditions

Temperature30 °C

Reaction Steps

200 g of benzyl 2,3-dihydro-1H-indole-2-carboxylate para-toluenesulphonate, 66 ml of triethylamine and 1 litre of ethyl acetate are introduced into a stirred reactor, followed, after stirring for 10 minutes at ambient temperature, by 89 g of N-[tert-butyloxycarbonyl]-(S)-alanine and 151 g of O-(benzotriazol-1-yl)-1,1,3,3-bis(tetramethylene)uronium tetrafluoroborate. The heterogeneous mixture is then heated at 30° C. for 3 hours whilst stirring well and is then cooled to 0° C. and filtered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288661B2
Source datasetuspto-grants-2007_10
ORD IDord-e88658cd9a99402083b0ebd33e439cd4
Source noteuspto-grants-2007_10