HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481442Generated: October 26, 2026
HCID 19066320, compound → HCID 178501432, compound
https://huagongshe.com/reaction/481442
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 19066320 | HCID 19066320 | — |
| Reactant | methyl (2S)-2-amino-4-(1H-1,2,3,4-tetrazol-5-yl)butanoate | HCID 178501500 | — |
| Product | HCID 178501432 | HCID 178501432 | 73% |
Reaction Steps
Using analogous procedures to those described in the second and third paragraphs of Example 12, pentafluorophenyl o-fluoro-p-[N-methyl-N-((6RS)-2-methyl-4-oxo-3-pivaloyloxymethyl-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)amino]benzoate was reacted with methyl (2S)-2-amino-4-(tetrazol-5-yl)butyrate to give methyl (2S)-2-{o-fluoro-p-[N-methyl-N-((6RS)-2-methyl-3-pivaloyloxymethyl-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)amino]benzamido}-4-(tetrazol-5-yl)butyrate in 73% yield which in turn was hydrolysed with aqueous sodium hydroxide solution to give (2S)-2-{o-fluoro-p-[N-methyl-N-((6RS)-2-methyl-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)amino]benzamido}-4-(tetrazol-5-yl)butyric acid in 81% yield, m.p. 203°-205° C.;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05789417 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-b40919c73043490097f4546075ea6c6a |
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| Source note | uspto-grants-1998_08 |
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