HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837571Generated: October 30, 2026
4-Toluenesulfonyl chloride → HCID 10024938, compound
https://huagongshe.com/reaction/1837571
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 22479020 | HCID 22479020 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10024938 | HCID 10024938 | — |
Reaction Steps
Concentrated ammonium hydroxide (35 mL) was added with stirring to a solution of N-[3-(2-butyl-5-oxido-1H-imidazo[4,5-c]quinolin-1-yl)propyl]-N′-phenylurea (2.25 g, 5.39 mmol) in dichloromethane (100 mL). Tosyl chloride (1.13 g,5.93 mmol) was added in small portions over a period of 30 minutes. After 1 hour the layers were separated. The aqueous layer was extracted with dichloromethane (2×25 mL). The organics were combined and extracted with water (3×50 mL). The aqueous layers were combined and filtered to provide 1.64 g of an off white solid. This material was recrystallized sequentially from 1,2-dichloroethane, isopropyl alcohol and methanol to provide 960 mg of N-[3-(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)propyl]-N′-phenylurea as light tan needles, m.p. 191-192° C. Analysis: Calculated for C24H28N6O: %C, 69.21; %H, 6.78; %N, 20.18; Found: %C; 68.94; %H, 6.77; %N, 19.90.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06784188B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-a4a1ed9efdf94b3993ffb2d4234d352a |
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| Source note | uspto-grants-2004_08 |
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