HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516471Generated: October 25, 2026
Acetone → (2R,4R)-4-[(1-Butyryloxymethoxy-1H-[1,2,3]triazole-4-carbonyl)amino]-5-(5'-chloro-2'-fluorobiphenyl-4-yl)-2-hydroxypentanoic Acid
https://huagongshe.com/reaction/516471
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chloromethyl butanoate | HCID 2725008 | — |
| Reactant | (2R,4R)-5-(5'-Chloro-2'-fluorobiphenyl-4-yl)-2-hydroxy-4-[(1-hydroxy-1H-[1,2,3]triazole-4-carbonyl)amino]pentanoic Acid | HCID 67969390 | — |
| Product | (2R,4R)-4-[(1-Butyryloxymethoxy-1H-[1,2,3]triazole-4-carbonyl)amino]-5-(5'-chloro-2'-fluorobiphenyl-4-yl)-2-hydroxypentanoic Acid | HCID 86705159 | 16.4% |
Reaction Steps
Chloromethyl butyrate (13.7 mg, 100 μmol) was added to a solution of (2R,4R)-5-(5′-chloro-2′-fluorobiphenyl-4-yl)-2-hydroxy-4-[(1-hydroxy-1H-1,2,3-triazole-4-carbonyl)amino]pentanoic acid (30.0 mg, 66.8 μmol) in acetone (0.5 mL, 6.8 mmol). Et3N (18.6 μL, 134 μmol) was added and the resulting mixture was stirred at 65° C. for 2 hours. The mixture was then concentrated in vacuo to yield a yellow liquid. The crude liquid was purified (preparative scale C18 column chromatography, small column, using 30-90% MeCN in water with 0.05% TFA) to yield the title compound as a white solid (6.0 mg). MS m/z [M+H]+ calc'd for C25H26ClFN4O7, 549.15. found 549.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108934B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-028a2fca226e4dd79d571027a3a5fdef |
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| Source note | uspto-grants-2015_08 |
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