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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608648Generated: October 31, 2026

Glutaric anhydride → HCID 23367636, compound

https://huagongshe.com/reaction/1608648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlutaric anhydrideHCID 7940—
ReactantHCID 23367631HCID 23367631—
ReactantHCID 23367634HCID 23367634—
ProductHCID 23367636HCID 23367636—

Reaction Steps

These materials were prepared using the procedures outlined in steps 2 and 3 of Example 2, except starting with 5-[4-(benzyloxycarbonyl)piperazinocarbonyl]-5H-dibenzo[b,f]azepine in place of the N-[3-(benzyloxycarbonylamino)propyl]carbamazepine in step 2, and thus the product 5-(Piperazinocarbonyl)-5H-dibenzo-[b,f]azepine Hydrobromide in place of the product of step 2, and glutaric anhydride in place of succinic anhydride in the procedures of step 3. The residue (2B) was crystallized from ethyl acetate (10 mL) and petroleum ether (2 mL), placed in a freezer, and filtered to give the acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05395933
Source datasetuspto-grants-1995_03
ORD IDord-ddfb9f8245274cb8adc25bb6c9fe5478
Source noteuspto-grants-1995_03