HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 5-{5-[4-(Ethyloxy)-3,5-difluorophenyl]-1,2,4-oxadiazol-3-yl}isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 4-Ethoxy-3,5-difluorobenzoic acid | HCID 46737603 | — |
| Reactant | HCID 178513273 | HCID 178513273 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-{5-[4-(Ethyloxy)-3,5-difluorophenyl]-1,2,4-oxadiazol-3-yl}isoquinoline | HCID 44476491 | 5.8% |
Reaction Steps
A mixture of 4-(ethyloxy)-3,5-difluorobenzoic acid (JRD Fluorochemicals Ltd; 130 mg, 0.641 mmol), HATU (244 mg, 0.641 mmol), Hunig's base (0.3 mL, 1.718 mmol) in N,N-dimethylformamide (DMF) (1 ml) was stirred at room temperature for 1 hr before the addition of N-hydroxy-5-isoquinolinecarboximidamide (D1; 100 mg, 0.534 mmol) in N,N-dimethylformamide (DMF) (1 ml). The reaction mixture was stirred at room temperature for 2-3 hrs and then heated in a microwave at 140° C. for 1.5 hr. The reaction mixture was concentrated in vacuo and purified by preparative HPLC (Waters Atlantis column, eluting with solvents A/B (A: Water+0.1% Formic acid, B: MeCN+0.1% Formic acid)) to give the title compound (11 mg)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08329730B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-86653cf6080a474fb54d01a192077af1 |
| Source note | uspto-grants-2012_12 |