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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41562Generated: October 28, 2026

tert-butyl 4-allyl-4-(N-((1-tosyl-1H-indol-4-yl)methyl)acrylamido)piperidine-1-carboxylate → tert-butyl 2-oxo-1-((1-tosyl-1H-indol-4-yl)methyl)-1,9-diazaspiro[5.5]undec-3-ene-9-carboxylate

https://huagongshe.com/reaction/41562

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-allyl-4-(N-((1-tosyl-1H-indol-4-yl)methyl)acrylamido)piperidine-1-carboxylateHCID 67251369—
CatalystHCID 178425456HCID 178425456—
SolventDichloromethaneHCID 6344—
Producttert-butyl 2-oxo-1-((1-tosyl-1H-indol-4-yl)methyl)-1,9-diazaspiro[5.5]undec-3-ene-9-carboxylateHCID 6725185884%

Reaction Steps

To a solution of tert-butyl 4-allyl-4-(N-((1-tosyl-1H-indol-4-yl)methyl)acrylamido)piperidine-1-carboxylate (0.075 g, 0.13 mmol) in dichloromethane (5.0 mL) was added Grubbs 2nd generation catalyst (0.006 g, 0.006 mmol) under argon and the reaction mixture was stirred at it overnight. The dark brown solution was concentrated under reduced pressure and the crude product was purified by column chromatography (eluent: 25% ethyl acetate in hexane) to yield the title compound as a solid (0.060 g, 84%). [LCMS RtE=0.523 min, [M+H]+=549.8]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530648B2
Source datasetuspto-grants-2013_09
ORD IDord-e407ce95cc794e2ab0b69b333ca3446e
Source noteuspto-grants-2013_09