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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378251Generated: November 3, 2026

N-Phthaloylglycine → HCID 67713329, compound

https://huagongshe.com/reaction/1378251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-PhthaloylglycineHCID 20825—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 67713483HCID 67713483—
SolventDimethylformamideHCID 6228—
ProductHCID 67713329HCID 67713329100%

Reaction Steps

A solution of 1.0 g (4.9 mmol) of N-phthaloylglycine in 8 ml of dimethylformamide was treated at room temperature with 0.83 g is (5.11 mmol) of 1,1'-carbonyldiimidazole and the mixture was subsequently heated to 50°. After 30 minutes the mixture was cooled to room temperature, 1.5 g (5 mmol) of (S)-10,11,12,12a-tetrahydro-8-oxo-8H-imidazo[5,1-c]pyrrolo[1,2-a]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 colourless powder obtained was washed with ethanol and diethyl ether. There were obtained 2.2 g (100%) of (S)-N'-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-ylacetyl)-8-oxo-10,11,12,12a-tetrahydro-8H-imidazo[5,1-c]pyrrolo[1,2-a]thieno[3,2-e][1,4]diazepine-1-carboxylic acid hydrazide of m.p. >260°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-4ff756c2aeba4ec8880d7adb07891b69
Source noteuspto-grants-1997_09