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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003990Generated: November 2, 2026

Triethylamine → 1-(t-Butyloxycarbonyl)-4-(4-morpholinecarbonyl)-1,4-diazepane

https://huagongshe.com/reaction/1003990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Morpholinecarbonyl chlorideHCID 84810—
ReactantTert-butyl 1,4-diazepane-1-carboxylateHCID 2756058—
SolventDichloromethaneHCID 6344—
Product1-(t-Butyloxycarbonyl)-4-(4-morpholinecarbonyl)-1,4-diazepaneHCID 1553828598.3%

Reaction Steps

A solution of 1-(t-butyloxycarbonyl)-1,4-diazepane (92.0 g, 0.46 mol) and triethylamine (96.0 ml, 69.7 g, 0.69 mol) in dichloromethane (500 ml) at 0° C. was treated dropwise with a solution of 4-morpholinecarbonyl chloride (64.0 ml, 82.0 g, 0.55 mol) in dichloromethane (100 ml) and the reaction was stirred at room temperature under nitrogen for 18 hours. The reaction mixture was then diluted with dichloromethane (400 ml) and washed with 2N citric acid (3×400 ml), saturated brine (1×500 ml), dried over MgSO4 and evaporated to give the subtitle compound as an off-white solid (141.7 g, 98%). Rf 0.80 (0.880 aqueous ammonia:methanol:dichloromethane 1:10:90, v/v). MS m/z 314 (MH)+. Found: C,57.50; H,8.69; N,13.41; C15H27N3O4 requires C, 57.50; H, 8.69; N,13.41%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06048864
Source datasetuspto-grants-2000_04
ORD IDord-46ff98b306ef40b6a385b366f0145213
Source noteuspto-grants-2000_04