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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946641Generated: October 28, 2026

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

https://huagongshe.com/reaction/1946641

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 numberUS08399452B2
Source datasetuspto-grants-2013_03
ORD IDord-fe4825a425f546a1b2849b214977a74c
Source noteuspto-grants-2013_03