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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357792Generated: November 1, 2026

Tripropylamine → 1-(4-Methoxy-benzenesulfonyl)-3-(4-methoxy-benzyloxycarbonyl-amino)-2,3,4,7-tetrahydro-1H-azepine-2-carboxylic Acid Tert-Butyl Ester

https://huagongshe.com/reaction/1357792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTripropylamineHCID 7616—
Reactant4-Methoxybenzyl alcoholHCID 7738—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant1-(4-Methoxy-benzenesulfonyl)-2,3,4,7-tetrahydro-1H-azepine-2,3-dicarboxylic acid 2-tert-butyl esterHCID 15550523—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Methoxy-benzenesulfonyl)-3-(4-methoxy-benzyloxycarbonyl-amino)-2,3,4,7-tetrahydro-1H-azepine-2-carboxylic Acid Tert-Butyl EsterHCID 15550525—

Reaction Steps

The reaction is performed under an Argon atmosphere and exclusion of light. 1-(4-Methoxy-benzenesulfonyl)-2,3,4,7-tetrahydro-1H-azepine-2,3-dicarboxylic acid 2-tert-butyl ester (550 mg, 1.34 mmol) is dissolved in 7 ml dry Tetrahydrofuran (THF). Tripropyl amine (TPA) (280 μl, 1.47 mmol) is added and the reaction is stirred for 30 minutes at RT. Diphenyl phosphoryl azide (318 μl, 1.47 mmol) is added and the reaction is gradually heated to 40° C. for 3 h. The reaction temperature is then increased to reflux conditions for 6 h. The reaction mixture is allowed to cool to room temperature and 4-Methoxybenzylalcohol (184 μl, 1.47 mmol) is added. The reaction is heated to reflux over night. The solvent is evaporated. Flash-chromatography Hexane/Ethylacetate (2:1) afforded the product: Cal. 383.5 found (M)+ 383.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06593351B2
Source datasetuspto-grants-2003_07
ORD IDord-a68e7fd85c4f48dca9d0dc1ab925ef94
Source noteuspto-grants-2003_07