HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518596Generated: October 30, 2026
Benzoyl isothiocyanate → HCID 178501176, compound
https://huagongshe.com/reaction/518596
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl isothiocyanate | HCID 68284 | — |
| Reactant | HCID 178501200 | HCID 178501200 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178501176 | HCID 178501176 | 17% |
Reaction Steps
To a solution of cis-methyl 4-(3-aminopyridin-4-ylamino)cyclohexanecarboxylate (70 mg, 0.281 mmol) in ACN (5.6 mL) under nitrogen was added benzoyl isothiocyanate (0.045 mL, 0.337 mmol). The reaction mixture was stirred for 30 minutes at RT. To the mixture was added polymer-supported-carbodiimide (936 mg, 1.123 mmol; Loading: 1.2 mmol/g;), and the resulting mixture was stirred at 70° C. for 16 hours. The reaction mixture was cooled to RT and filtered, and the resin was washed with 1% MeOH/DCM. The filtrate was concentrated and purified by silica gel chromatography (1-4% MeOH/DCM) to afford cis-methyl 4-((E)-2-(benzoylimino)-2,3-dihydro-1H-imidazo[4,5-c]pyridin-1-yl)cyclohexanecarboxylate as an off-white solid (18 mg, 17% yield). MS m/z=379.2 [M+H]. Calc'd for C21H22N4O3: 378.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115127B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-dec93dd54fa84194b26ae356a1a11dad |
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| Source note | uspto-grants-2015_08 |
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