HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667631Generated: November 4, 2026
Tetrahydrofuran → ((S)-1-Cyclohexyl-2-{(S)-2-[2-(2,3-dihydro-indol-1-yl)-pyridin-4-yl]-pyrrolidin-1-yl}-2-oxo-ethyl)-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/1667631
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | (2S)-[[N-(tert-Butoxycarbonyl)-N-methyl-L-alanyl]amino](cyclohexyl)ethanoic acid | HCID 17748007 | — |
| Reactant | 4-(4,6-Dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrate | HCID 23149411 | — |
| Reactant | 3-((S)-5-Pyrrolidin-2-yl-pyridin-3-yl)-1H-indole | HCID 58111884 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | ((S)-1-Cyclohexyl-2-{(S)-2-[2-(2,3-dihydro-indol-1-yl)-pyridin-4-yl]-pyrrolidin-1-yl}-2-oxo-ethyl)-carbamic acid tert-butyl ester | HCID 66889172 | — |
Reaction Steps
To a solution of 3-((S)-5-Pyrrolidin-2-yl-pyridin-3-yl)-1H-indole 6 (78 mg, 0.30 mmole) and (S)-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-propionylamino]-cyclohexyl-acetic acid (111.6 mg, 0.33 mmole) in 5 ml of THF at 0° C., was added 4-(4,6-Dimethoxy-[1,3,5]triazin-2-yl)-4-methyl-morpholinium chloride hydrate (98.6 mg, 0.36 mmole) in one portion. After stirring at 20° C. for 2 hours, the reaction mixture was diluted with 30 mL of EtOAc, washed with 3×10 mL of water and concentration to give [(S)-1-(S)-1-Cyclohexyl-2-{(S)-2-[5-(1H-indol-3-yl)-pyridin-3-yl]-pyrrolidin-1-yl}-2-oxo-ethylcarbamoyl)-ethyl]-methyl-carbamic acid tert-butyl ester 7 (143.5 mg, crude) as pale yellow solid without further purification for next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044209B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-c13a2ef416dd4677814d79eb90e228d0 |
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| Source note | uspto-grants-2011_10 |
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