HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981659Generated: October 30, 2026
Diethyl azodicarboxylate → HCID 14989389, compound
https://huagongshe.com/reaction/981659
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | ethyl 4-mercaptobenzoate | HCID 10845149 | — |
| Reactant | HCID 14989224 | HCID 14989224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14989389 | HCID 14989389 | 13.5% |
Reaction Steps
To a stirred solution of 5.6 parts of 1-(6-chloro-3-pyridazinyl)-4-piperidinepropanol, 4.2 parts of ethyl 4-mercaptobenzoate and 6 parts of triphenylposphine in 135 parts of tetrahydrofuran was added dropwise a solution of 4 parts of diethyl diazenedicarboxylate in 45 parts of tetrahydrofuran at 20° C. Upon complete addition, stirring was continued overnight at this temperature. The reaction mixture was evaporated and the residue was taken up in water. The product was ectracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (99:1 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2,2'-oxybispropane. The product was filtered off and dried, yielding 1.3 parts (13.5%) of ethyl 4-[[3-[1-(6-chloro-3-pyridazinyl)-4-piperidinyl]propyl]thio]benzoate; mp. 96.3° C. (comp. 164).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04992433 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-635f8a4045eb4a5e960df0a16643ca88 |
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| Source note | uspto-grants-1991_02 |
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