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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Glycine | HCID 750 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Methylisatoic anhydride | HCID 25160 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 1-Methyl-3,4-dihydro-1H-1,4-benzodiazepine-2,5-dione | HCID 3562387 | 67.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399452B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-fe4825a425f546a1b2849b214977a74c |
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| Source note | uspto-grants-2013_03 |
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