HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 54358839, compound → (2S)-2-{p-[N-((6RS)-2-methyl-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]benzamido)pimelic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 54358839 | HCID 54358839 | — |
| Reactant | p-[N-((6RS)-2-Methyl-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]benzoic acid | HCID 135443466 | — |
| Product | (2S)-2-{p-[N-((6RS)-2-methyl-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]benzamido)pimelic acid | HCID 136351319 | 25% |
Reaction Steps
Using an analogous procedure to that described in Example 3, p-[N-((6RS)-2-methyl-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]benzoic acid was coupled to diethyl (2S)-2-aminopimelate (J. Med. Chem., 1983, 26, 1719) and the resultant product was hydrolysed to give (2S)-2-{p-[N-((6RS)-2-methyl-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]benzamido)pimelic acid in 25% yield, m.p. 165° C.;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05789417 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-7d261a156aaa477695e0939fc7bfaa76 |
| Source note | uspto-grants-1998_08 |