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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375354Generated: November 2, 2026

Propanedioyl dichloride → tert-butyl (2,4-dioxo-5-phenyl-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-1-yl)acetate

https://huagongshe.com/reaction/1375354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropanedioyl dichlorideHCID 74269—
Reactanttert-butyl N-(2-anilinophenyl)glycinateHCID 69425039—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl (2,4-dioxo-5-phenyl-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-1-yl)acetateHCID 86602389—

Reaction Steps

To 100 mL of THF at 0° C. was added dropwise over 20 min simultaneously a solution of the tert-butyl N-(2-anilinophenyl)glycinate (9.5 g, 31.8 mM) in 100 mL of THF and solution of malonyl dichloride (5.38 mL, 38.21 mM) in 100 mL of THF. The resulting solution was stirred at RT for 20 h and the solvent removed in vacuo. The resultant material was purified by silica gel flash column chromatography using hexanes/EtOAc 6/14 and the combined filtrates evaporated in vacuo to give 10.2 g of product. 1H NMR (DMSO-d6) 1.40 (s, 9H), 3.19 (d, J=12 Hz, 1H), 3.69 (d, J=12 Hz, 1H), 4.55 (d, J=17 Hz, 1H), 4.71 (d, J=17 Hz, 1H), 6.89 (d, J=8 Hz, 1H), 7.20 (t, J=8 Hz, 1H), 7.33 (m, 4H), 7.46 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169773B2
Source datasetuspto-grants-2007_01
ORD IDord-678afc13401744dc8b7cabd8de2e9a1e
Source noteuspto-grants-2007_01