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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101223Generated: October 25, 2026

N,N,N',N'-Tetramethylazodicarboxamide → Tert-butyl 2-({6-[(tert-butoxycarbonyl)amino]pyridin-3-yl}methyl)-3-[(4-methoxybenzyl)thio]-5-[3-(tetrahydrofuran-3-yloxy)phenyl]pentanoate

https://huagongshe.com/reaction/2101223

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylazodicarboxamideHCID 4278—
Reactant3-Furanol, tetrahydro-HCID 9960—
ReactantTributylphosphineHCID 13831—
ReactantTert-butyl 2-({6-[(tert-butoxycarbonyl)amino]pyridin-3-yl}methyl)-5-(3-hydroxyphenyl)-3-[(4-methoxybenzyl)thio]pentanoateHCID 69072041—
SolventTolueneHCID 1140—
ProductTert-butyl 2-({6-[(tert-butoxycarbonyl)amino]pyridin-3-yl}methyl)-3-[(4-methoxybenzyl)thio]-5-[3-(tetrahydrofuran-3-yloxy)phenyl]pentanoateHCID 6907320044.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

1,1′-azobis(N,N-dimethylformamide)(134 mg, 0.78 mmol) was added to a solution of tri-n-butylphosphine (221 μL, 0.89 mmol) in toluene (2 mL). Tetrahydrofuran-3-ol (36 μL, 44 mmol) and tert-butyl 2-({6-[(tert-butoxycarbonyl)amino]pyridin-3-yl}methyl)-5-(3-hydroxyphenyl)-3-[(4-methoxybenzyl)thio]pentanoate (154 mg, 0.25 mmol) was added sequentially. The reaction mixture was stirred for 12 h at 80° C. Toluene (100 mL) was added and the mixture was washed with brine, dried and concentrated. Flash chromatography (toluene/EtOAc, 100:0 to 70:30) gave tert-butyl 2-({6-[(tert-butoxycarbonyl)amino]pyridin-3-yl}methyl)-3-[(4-methoxybenzyl)thio]-5-[3-(tetrahydrofuran-3-yloxy)phenyl]pentanoate (75 mg, 35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572817B2
Source datasetuspto-grants-2009_08
ORD IDord-e63b0239c61f48d596a027b78ddab03d
Source noteuspto-grants-2009_08