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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718111Generated: October 29, 2026

Glycine → 1-Methyl-3,4-dihydro-1H-1,4-benzodiazepine-2,5-dione

https://huagongshe.com/reaction/718111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycineHCID 750—
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantN-Methylisatoic anhydrideHCID 25160—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
Solvent1,2-DimethoxyethaneHCID 8071—
Product1-Methyl-3,4-dihydro-1H-1,4-benzodiazepine-2,5-dioneHCID 356238767.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

1-Methyl-1H-benzo[d][1,3]oxazine-2,4-dione (11.0 g, 62.1 mmol) and 2-aminoacetic acid (5.13 g, 68.3 mmol) were dissolved in DME (60 mL) and water (20 mL) and triethylamine was added. The reaction mixture was stirred at 60° C. for 4 hours. The mixture was concentrated in vacuo to get a light tan heavy oily residue that was dissolved in acetic acid (75 mL). This mixture was refluxed 4 hours then cooled down to room temperature. The solvent was evaporated to get a tan heavy oil. The oil was allowed to stand at room temperature overnight in ether (50 mL). The beige crystalline solid was filtered and washed with ether. The solid was then triturated in ether to afford title compound 467 (7.95 g, 67%) as a beige crystalline solid. 1H NMR (DMSO-d6) δ (ppm): 8.70 (s, 1H), 7.70 (d, J=7.6 Hz, 1H), 7.60 (t, J=7.2 Hz, 1H), 7.42 (d, J=8.0 Hz, 1H), 7.32 (t, J=7.5 Hz, 1H), 3.75-3.72 (m, 1H), 3.51-3.46 (m, 1H), 3.28 (s, 3H). MS (ESI): 190.90 (MH)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193749B2
Source datasetuspto-grants-2015_11
ORD IDord-aa5c6682a1d04c6e935117a06971d5b2
Source noteuspto-grants-2015_11