HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908613Generated: October 28, 2026
Triphenylphosphine → 4-{(S)-4-Carboxy-2-[(5-cyclobutoxy-1-phenyl-1H-pyrazole-3-carbonyl)-amino]butyryl}-piperazine-1-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1908613
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Cyclobutanol | HCID 76218 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 178473388 | HCID 178473388 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-{(S)-4-Carboxy-2-[(5-cyclobutoxy-1-phenyl-1H-pyrazole-3-carbonyl)-amino]butyryl}-piperazine-1-carboxylic acid ethyl ester | HCID 44126405 | — |
Reaction Steps
To a solution of 50 mg of 4-{(S)-4-tert-Butoxycarbonyl-2-[(5-hydroxy-1-phenyl-1H-pyrazole-3-carbonyl)-amino]-butyryl}-piperazine-1-carboxylic acid ethyl ester and 8 mg of Cyclobutanol in 2 ml of THF, 37 mg of polymerbound triphenyl phosphine (Fluka, 3 mmol triphenylphosphine/g resin) and 20 mg of Diethyl azodicarboxylate was added and stirred for 16 h. Then, the reaction mixture was filtered and the solvents were removed under reduced pressure. The residue was dissolved in 1 ml of DCM and 0.2 ml TFA. After 4 h 10 ml of toluene was added and the solvents were removed under reduced pressure. The residue was purified by preparative HPLC (C18 reverse phase column, elution with a water/MeCN gradient with 0.1% TFA). The fractions containing the product were evaporated and lyophilized to yield a white solid. Yield: 2 mg MS (ES+): m/e=528.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598179B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-d9de045fbb2d4b668f5b1ce3b1c3287a |
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| Source note | uspto-grants-2013_12 |
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