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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tert-butoxycarbonylalanine | HCID 85082 | — |
| Reactant | benzyl 2,3-dihydro-1H-indole-2-carboxylate para-toluenesulphonate | HCID 86612765 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | benzyl (2S)-1-{(2S)-2-[(tert-butoxycarbonyl)amino]propionyl}-2,3-dihydro-1H-indole-2-carboxylate | HCID 86612047 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07288661B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-e88658cd9a99402083b0ebd33e439cd4 |
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| Source note | uspto-grants-2007_10 |
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