HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 178511229, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 178508823 | HCID 178508823 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178511229 | HCID 178511229 | — |
Reaction Steps
A solution of trans-{4-[4-amino-5-(4-phenoxy-phenyl)-imidazo[5,1-f][1,2,4]triazin-7-yl]-cyclohexylmethyl}-carbamic acid benzyl ester (20.0 mg, 0.0364 mmol) and 4 M of HCl in 1,4-dioxane (2 mL) was heated to reflux overnight. The solution was concentrated in vacuo and left to dry in the vacuum oven overnight to afford the title compound as a yellow solid. 1H NMR (400 MHz, CDCl3): δ=1.23-1.37 (m, 2H), 1.83-1.99 (m, 3H), 2.03-2.09 (m, 2H), 2.15-2.24 (m, 2H), 2.86 (d, J=4.0 Hz, 2H), 3.44-3.56 (m, 1H), 7.12 (d, J=8.1 Hz, 2H), 7.17-7.26 (m, 3H), 7.44 (t, J=7.8 Hz, 3H), 7.66 (d, J=3.5 Hz, 2H), 8.00-8.10 (m, 1H). MS (ES+): m/z 415.02 (100) [MH+]. HPLC: tR=2.26 min (OpenLynx, polar—5 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08481733B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-a3888b8a5e094e2f8658f7c4b0111f76 |
| Source note | uspto-grants-2013_07 |