HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105492Generated: November 3, 2026
Trichloroacetyl isocyanate → HCID 57538842, compound
https://huagongshe.com/reaction/2105492
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trichloroacetyl isocyanate | HCID 76400 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 67506136 | HCID 67506136 | — |
| Product | HCID 57538842 | HCID 57538842 | 28% |
Reaction Steps
The methods described in Parts C and D of Example 20 were used to oxidize and aminate 2-butyl-1-methoxy-1H-imidazo[4,5-c]quinoline (3.2 g, 12.5 mmol) with the following modifications. The oxidation reaction was stirred for two hours at room temperature. The reaction with trichloroacetyl isocyanate (2.2 mL, 19 mmol) was carried out at room temperature overnight, and the reaction sodium methoxide was stirred overnight and then concentrated under reduced pressure. The residue was treated with methanol (5 mL) to form a solid, which was collected by filtration and recrystallized from methanol/water and dried overnight in a vacuum oven at 70° C. to provide 0.946 g of 2-butyl-1-methoxy-1H-imidazo[4,5-c]quinolin-4-amine as golden crystals, mp 197-199° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07579359B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-969789d85d4b49b3a91f454b55873da7 |
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| Source note | uspto-grants-2009_08 |
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