HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069055Generated: October 31, 2026
1,1'-Carbonyldiimidazole → HCID 58532566, compound
https://huagongshe.com/reaction/2069055
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 3-tert-butyl-1-(4-methylphenyl)-1H-pyrazol-5-amine | HCID 2974132 | — |
| Reactant | HCID 58532571 | HCID 58532571 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58532566 | HCID 58532566 | 40.9% |
Reaction Steps
A solution of 3-tert-butyl-1-p-tolyl-1H-pyrazol-5-amine (5) (212 mg, 0.923 mmol) in DCM (1 mL) was added to a stirred solution of CDI (150 mg, 0.923 mmol) in DCM (1 mL), under nitrogen at RT over 5 min. After 1.5 hr a solution of tert-butyl 4-(2-(4-aminonaphthalen-1-yloxy)propyl)pyridin-2-ylcarbamate (49) (242 mg, 0.615 mmol) in DCM (2 mL) was added and stirring was continued at RT for 16 hr. A second portion of 3-tert-butyl-1-p-tolyl-1H-pyrazol-5-amine (141 mg, 0.615 mmol) in DCM (1 mL) was processed in a similar manner to the first, by reaction with CDI (100 mg, 0.615 mmol) in DCM (1 mL) and the resulting adduct was then added to the reaction mixture. After a further 2.5 hr the mixture was partitioned between water and DCM. The aqueous layer was extracted with DCM and the combined organic extracts were washed with brine and then dried (MgSO4) and evaporated in vacuo. The residue was purified by flash column chromatography (SiO2, 40 g, 0-100% EtOAc in isohexane, gradient elution) to afford the title compound (50) (163 mg, 40%) as a purple foam: m/z 649 (M+H)+ (ES+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299073B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-7e9bb84c4cd3446f9606754a19d7549e |
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| Source note | uspto-grants-2012_10 |
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