HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378255Generated: October 30, 2026
N-Phthaloylglycine → HCID 67713642, compound
https://huagongshe.com/reaction/1378255
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Phthaloylglycine | HCID 20825 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 67713661 | HCID 67713661 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67713642 | HCID 67713642 | 96.1% |
Reaction Steps
A solution of 5.8 g (19 mmol) of N-phthaloylglycine in 30 ml of dimethylformamide was treated at room temperature with 3.2 g (19.75 mmol) of 1,1'-carbonyldiimidazole and the mixture was subsequently heated to 50°. After 30 minutes the mixture was cooled to room temperature, 5.6 g (19.63 mmol) of (S)-8-oxo-11,11 a-dihydro-8H,10H-azeto[1,2-a]imidazo[5,1-c]thieno-[3,2-e][1,4]diazepine-1-carboxylic acid hydrazide were added thereto and the mixture was stirred at room temperature for 12 hours. The suspension obtained was filtered and the colour-less powder obtained was washed with ethanol and diethyl ether. There were obtained 8.7 g (96%) of (S)-N'-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-ylacetyl)-8-oxo-11,11a-dihydro-8H,10H-azeto [1,2-a]imidazo[5,1-c]thieno[3,2-e][1,4]diazepine-1-carboxylic acid hydrazide of m.p. >260°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05665718 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-8c56a6b78cbc493ab31fa77a7af5a6bf |
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| Source note | uspto-grants-1997_09 |
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