HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 178502054, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 3,4-Diaminoquinoline | HCID 1514289 | — |
| Reactant | N-carbomethoxy-S-methylisothiourea | HCID 145796808 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178502054 | HCID 178502054 | — |
Reaction Steps
To a solution of 6.6 g (0.041 mole) of 3,4-diaminoquinoline (from Example 39), 2.0 ml of glacial acetic acid, 35 cc of ethanol and 35 ml of water was added 9.3 g (0.045 mole) of N-carbomethoxy-S-methylisothiourea, and the mixture was heated at its reflux temperature for two hours. Evaporation provided a residue which was suspended in ethanol, separated by filtration and washed with water. Recrystallization from ethanol provided methyl 1H-imidazo[4,5-c]quinolin-2-carbamate hydrate, m.p. >250° C. Analysis: Calculated for C12H10N4O2. 0.75H2O: %C, 56.4; %H, 4.5; %N, 21.9; Found: %C, 56.1; %H, 4.4; %N, 22.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04698348 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-0e2730d88efe48169e176305209b589a |
| Source note | uspto-grants-1987_10 |