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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41548Generated: October 28, 2026

Acryloyl chloride → tert-butyl 4-allyl-4-(N-((1-tosyl-1H-indol-4-yl)methyl)acrylamido)piperidine-1-carboxylate

https://huagongshe.com/reaction/41548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcryloyl chlorideHCID 13140—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-butyl 4-allyl-4-((1-tosyl-1H-indol-4-yl)methylamino)piperidine-1-carboxylateHCID 67252109—
SolventDichloromethaneHCID 6344—
Producttert-butyl 4-allyl-4-(N-((1-tosyl-1H-indol-4-yl)methyl)acrylamido)piperidine-1-carboxylateHCID 6725136972.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Acryloyl chloride (0.360 g, 0.401 mmol) was added at 0° C. to a stirred solution of tert-butyl 4-allyl-4-((1-tosyl-1H-indol-4-yl)methylamino)piperidine-1-carboxylate (0.2 g, 0.382 mmol), diisopropylethylamine (0.32 mL, 1.91 mmol) in DCM (5.0 mL). The reaction mixture was stirred at 0° C. for 30 min and was then allowed to warm to rt and stirred for 4 h. The reaction mixture was concentrated under reduced pressure and the crude product was purified by column chromatography (eluent: 5% ethyl acetate in hexane) to yield the title compound as a white solid (0.16 g, 72%). LCMS RtA=0.774, [M+H-Boc]+=477.9

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530648B2
Source datasetuspto-grants-2013_09
ORD IDord-c7ab213d3d8d4587ab244366e78e25ba
Source noteuspto-grants-2013_09