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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29757Generated: October 26, 2026

2-(2-tert-Butoxycarbonylamino-pyridin-4-ylmethylene)-succinic acid 4-benzyl ester 1-tert-butyl ester → 2-(2-Tert-butoxycarbonylamino-pyridin-4-ylmethyl)-succinic acid 1-tert-butyl ester

https://huagongshe.com/reaction/29757

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-tert-Butoxycarbonylamino-pyridin-4-ylmethylene)-succinic acid 4-benzyl ester 1-tert-butyl esterHCID 54209259—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-(2-Tert-butoxycarbonylamino-pyridin-4-ylmethyl)-succinic acid 1-tert-butyl esterHCID 6930298583%

Reaction Steps

2-(2-tert-Butoxycarbonylamino-pyridin-4-ylmethylene)-succinic acid 4-benzyl ester 1-tert-butyl ester (2.81 g, 7.60 mmol) and Pd/C (10%, 400 mg) were suspended in EtOH and hydrogenated at 41 atm. and 28° C. for 3 days. The catalyst was removed from the reaction mixture by filtration. The catalyst was washed with EtOH (96%). 1 M K2CO3 (30 mL) was added to the filtrate followed by addition of water (50 mL). After 2 days the reaction mixture was evaporated to ca 80 mL, then brine (10 mL) was added and the reaction mixture extracted with ether. The aqueous phase was acidified to pH=3 and extracted with chloroform. Methanol (25 mL) was added and the reaction mixture was dried (Na2SO4+CaSO4) and filtered to give 2-(2-tert-butoxycarbonylamino-pyridin-4-ylmethyl)-succinic acid 1-tert-butyl ester (1.90 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423012B2
Source datasetuspto-grants-2008_09
ORD IDord-00b62a1f34d149f5be38cda9b8af03bf
Source noteuspto-grants-2008_09