HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → 2'-Phthalimidomethylbiphenyl-2-carboxylic acid benzylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2'-Phthalimidomethylbiphenyl-2-carboxylic acid | HCID 14258571 | — |
| Product | 2'-Phthalimidomethylbiphenyl-2-carboxylic acid benzylamide | HCID 67318032 | — |
Reaction Steps
From 2′-phthalimidomethylbiphenyl-2-carboxylic acid (precursor 2), after conversion into the acid chloride using thionyl chloride and reaction with benzylamine, 2′-phthalimidomethylbiphenyl-2-carboxylic acid benzylamide was obtained. 1.2 g (2.7 mmol) of the product were dissolved in 55 ml of methanol and treated with 1.35 ml of hydrazine hydrate. After stirring at 40° C. for 1 h, the reaction mixture was concentrated and the residue was taken up in methylene chloride. After filtering off the 2,3-dihydrophthalazine-1,4-dione formed, the mother liquor was concentrated and the residue was purified by flash chromatography using methylene chloride/methanol 30:1. 0.49 g of 2′-aminomethylbiphenyl-2-carboxylic acid benzylamide was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07982045B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-f667c5f399c4414ba940e5e270afc9e0 |
| Source note | uspto-grants-2011_07 |