HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Ethylhexanoyl chloride → HCID 23512710, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Ethylhexanoyl chloride | HCID 79103 | — |
| Reactant | 1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amine | HCID 15453775 | — |
| Product | HCID 23512710 | HCID 23512710 | — |
Reaction Steps
According to the general method of Example 14, 1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amine and 2-ethylhexanoyl chloride were combined to provide N1-[4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-2-ethylhexanamide as a tan powder, m.p. 163.0-164.0° C. 1H NMR (300 MHz, DMSO-d6) δ 8.19 (s, 1H), 8.03 (d, J=8.1 Hz, 11H), 7.79 (m, 11H), 7.61 (dd, J=8.1, 1.2 Hz 11H), 7.44 (dt, J=7.5, 1.2 Hz, 11H), 7.26 (dt, J=7.5, 1.2 Hz, 11H), 6.63 (s, 2H), 4.61 (t, J=6.9 Hz, 2H), 3.12-3.05 (m, 2H), 1.94-1.82 (m, 3H), 1.49-1.03 (m, 10H), 0.76 (t, J=7.2 Hz, 3H), 0.67 (t, J=7.2 Hz, 3H); MS (EI) m/e 381.2533 (381.2529 calcd for C22H31N5O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07393859B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-f62093a7f3ae4c44ab8f89b517218593 |
| Source note | uspto-grants-2008_07 |