HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycine → Acetic acid, 2-((2-chlorobenzoyl)amino)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glycine | HCID 750 | — |
| Reactant | 2-Chlorobenzoyl chloride | HCID 69110 | — |
| Product | Acetic acid, 2-((2-chlorobenzoyl)amino)- | HCID 177756 | — |
Reaction Steps
Commercially available 2-chlorobenzoyl chloride was treated with glycine to give 2-(2-chlorobenzamido)acetic acid 21 in good yield. Then, 21 was reacted with acetic anhydride and benzaldehyde, in the presence of sodium acetate, to lead to the corresponding oxazolone in excellent yield. The resulting (4Z)-4-benzylidene-2-(2-chlorophenyl)oxazol-5(4H)-one 22 was converted via a Friedel-Crafts reaction to 1-(2-chlorophenyl)isoquinoline-3-carboxylic acid 23 in moderate yield2. Finally, the dimeric compounds 24 were easily obtained in good yields by transformation of the acid into acylchloride and further reactions with diamines.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541428B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-0265f1affbb64facaf2cf661fd11d395 |
| Source note | uspto-grants-2013_09 |