HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570644Generated: October 30, 2026
Benzylacetylene → Propyl [7-(5-benzyl-1H-1,2,3-triazol-1-yl)-4-fluoro-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl]acetate
https://huagongshe.com/reaction/570644
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzylacetylene | HCID 575753 | — |
| Reactant | Propyl (7-azido-4-fluoro-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl)acetate | HCID 86645392 | — |
| Catalyst | HCID 178425933 | HCID 178425933 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Propyl [7-(5-benzyl-1H-1,2,3-triazol-1-yl)-4-fluoro-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl]acetate | HCID 86645394 | — |
Reaction Steps
To a stirred solution of propyl (7-azido-4-fluoro-6,7,8,9-tetrahydropyrido[1,2-α]indol-10-yl)acetate (1 eq) and prop-2-yn-1-ylbenzene (1.5 eq) in benzene (0.3M) at room temperature was added chloro(1,5-cyclooctadiene) (pentamethylcyclopentadienyl)-ruthenium(II) (0.1 eq). The reaction mixture was flushed with nitrogen then aged at 80° C. for overnight, cooled to room temperature, filtered through silica gel, washed with EtOAc and concentrated. The residue was purified by column chromatography on silica gel eluting with EtOAc/Hexane (0 to 50%) to give the desired material as a brown oil. The racemic mixture was resolved by HPLC using a 50×400 mm Chiralpak AD column eluting with 15% MeOH, 15% EtOH, 69.75% Hexanes and 0.25% Et3N at 50 mL/min and 254 nm to afford the desired chiral ester with retention time of 9.6 and 11.6 min respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09023864B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-e1c5142f8439444a8b44d0f1018906d2 |
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| Source note | uspto-grants-2015_05 |
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