HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404466Generated: November 1, 2026
Diisopropylethylamine → HCID 178480515, compound
https://huagongshe.com/reaction/2404466
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N,N'-bis-Boc-guanylpyrazole | HCID 86695324 | — |
| Reactant | HCID 178480513 | HCID 178480513 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178480515 | HCID 178480515 | — |
Reaction Steps
To a solution of 2-{3-[(5-fluoro-1H-benzimidazol-2-yl)(1-methylpiperidin-4-yloxy)methyl]phenylsulfanyl}ethylamine (example 437B, 230 mg) in acetonitrile (15 mL) is added is added N,N′-bis-Boc-guanylpyrazole (172 mg) and diisopropylethylamine (1 equivalent) at room temperature. The mixture is stirred at room temperature for 3 h. The solvent and volatiles are removed under reduced pressure. The residue is purified by chromatography on silica gel (gradient dichloromethane/methanol from 100/0 to 95/5). The residue is then dissolved in 5N aqueous hydrochloric acid (8 mL) and the solution is stirred overnight at room temperature. The solvent and volatiles are removed under reduced pressure and the residue is triturated with diethyl ether and filtered to afford N-(2-{3-[(5-fluoro-1H-benzimidazol-2-yl)(1-methylpiperidin-4-yloxy)methyl]phenylsulfanyl}ethyl) guanidine trihydrochlorhide as a white crystalline solid melting at 170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802664B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-c661de69f91a47df819a5f618e2eddb1 |
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| Source note | uspto-grants-2014_08 |
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