HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220602Generated: November 1, 2026
Dichloromethane → 1-{4-[4-(1,5-Dimethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl-3'-yl]-benzyl}-pyrrolidine-2,5-dione hydrochloride
https://huagongshe.com/reaction/220602
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Succinimide | HCID 11439 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | {4-[4-(1,5-dimethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl-3'-yl]-phenyl}-methanol | HCID 59321924 | — |
| Product | 1-{4-[4-(1,5-Dimethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl-3'-yl]-benzyl}-pyrrolidine-2,5-dione hydrochloride | HCID 68597439 | — |
Reaction Steps
Dissolve succinimide (99 mg, 1.0 mmol) in dry DCM (5 mL) under nitrogen. Add triphenylphosphine (408 mg, 1.5 mmol) and stir for 20 min. at room temperature. Add {4-[4-(1,5-dimethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl-3′-yl]-phenyl}-methanol (378 mg, 1.0 mmol) and diethyl azodicarboxylate (0.19 mL, 1.1 mmol) and stir for 20 hr. Add water (10 mL), extract with DCM (2×5 mL). Pass the combined DCM extracts through an IST Phase Separator Frit®, concentrate and purify by SCX-2® chromatography washing with methanol then eluting with 2 M ammonia in methanol. Further purify (silica gel chromatography, eluting with 0:100 to 5:95 methanol:DCM), to give the free base as a light yellow oil. Purify again by low pH reverse phase HPLC, and form the free base by passing through an SCX-2® ion exchange cartridge washing with methanol then eluting with 3.5 M ammonia in methanol. Dissolve the oil in acetonitrile and convert to the hydrochloride salt by adding 2 M aq HCl solution. Add water and lyophilize to give the title compound as a yellow powder (127 mg, 26%). MS (ES): m/z=460 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202873B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-34dbc7c7f70049a49487920c3c4b2942 |
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| Source note | uspto-grants-2012_06 |
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