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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675417Generated: October 31, 2026

(2S,4R)-N-(hex-5-enyl)-4-hydroxy-N-methylpyrrolidine-2-carboxamide → (2S,4R)-2-N-(hept-6-enyl)-4-hydroxy-N-methylpyrrolidine-2-carboxamide

https://huagongshe.com/reaction/1675417

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S,4R)-N-(hex-5-enyl)-4-hydroxy-N-methylpyrrolidine-2-carboxamideHCID 57816715—
Reactant(2S,4R)-tert-butyl 2-(N-(hept-6-enyl)-N-methylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylateHCID 66650539—
Product(2S,4R)-2-N-(hept-6-enyl)-4-hydroxy-N-methylpyrrolidine-2-carboxamideHCID 6665066335%

Reaction Steps

Compound 71a was synthesized from compound 70a as yellow oil in 35% yield, following the procedure as described for compound 49.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003659B2
Source datasetuspto-grants-2011_08
ORD IDord-f16b4072fc654da694b2bea4f37b65b4
Source noteuspto-grants-2011_08