HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371309Generated: October 25, 2026
Propyl Isothiocyanate → N-[4-(4-amino-2-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-N'-propylthiourea
https://huagongshe.com/reaction/1371309
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propyl Isothiocyanate | HCID 69403 | — |
| Reactant | 1-(4-aminobutyl)-2-phenyl-1H-imidazo[4,5-c]quinolin-4-amine | HCID 12148992 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-[4-(4-amino-2-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-N'-propylthiourea | HCID 9954525 | 6.6% |
Reaction Steps
A solution of propyl isothiocyanate (0.78 g, 7.72 mmol) in chloroform (5 mL) was added at ambient temperature to a solution of 1-(4-aminobutyl)-2-phenyl-1H-imidazo[4,5-c]quinolin-4-amine (0.256 g, 7.72 mmol) in a mixture of chloroform (25 mL) and pyridine (5 mL). The reaction mixture was maintained at ambient temperature over the weekend. The reaction was quenched with ethanol and then concentrated under vacuum to provide a pale orange syrup. This material was purified by flash chromatography (silica gel, eluting with 10% methanol in dichloromethane). The pure fractions were combined and concentrated under vacuum to provide 0.22 g of N-[4-(4-amino-2-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-N′-propylthiourea as a white solid, m.p. 113–116° C. Mass spec M+1=433.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07157453B2 |
|---|
| Source dataset | uspto-grants-2007_01 |
|---|
| ORD ID | ord-9c77339e09194ecba97e92c4317ed771 |
|---|
| Source note | uspto-grants-2007_01 |
|---|