HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 5-(Bis-cyclopropylmethyl-amino)-5,6-dihydro-1H,4H-imidazo[4,5,1-ij]quinolin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | 5-Amino-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one | HCID 15937766 | — |
| Reactant | 6-Bromo-1,2,3,4-tetrahydro-8-nitro-3-quinolinamine dihydrochloride | HCID 19919357 | — |
| Product | 5-(Bis-cyclopropylmethyl-amino)-5,6-dihydro-1H,4H-imidazo[4,5,1-ij]quinolin-2-one | HCID 15745008 | — |
Reaction Steps
Following the procedure of Example 54, but substituting cyclopropylmethyl bromide for iodopropane and 5-(amino)-5,6-dihydro-4H-imidazo[4,5,1 -ij]quinolin-2(1H)-one for 6-bromo-1,2, 3,4-tetrahydro-8-nitro-3-quinolinamine dihydrochloride there were obtained 5-[bis(cyclopropylmethyl)amino]-5, 6-dihydro-4H-imidazo[4,5,1 -ij ]quinolin-2(1H)-one, mp 152-154 from ethyl acetate:hexane and 5 -(cyclopropylmethylamino)-5,6-dihydro-4H-imidazo [4,5,1 -ij]quinolin-2(1H) -one. The latter compound was converted to the hydrochloride salt, mp 309° C. from methanol:ether. ##STR2##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05436240 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-590a9bda83374fe2aa4b830101d0f761 |
| Source note | uspto-grants-1995_07 |