HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178458433, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-(Aminomethyl)-2-propoxyphenol hydrochloride | HCID 42625832 | — |
| Reactant | 4-methoxymethylene-6-pyrrol-1-yl-4H-isoquinoline-1,3-dione | HCID 68693125 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178458433 | HCID 178458433 | — |
Reaction Steps
A mixture of 5-aminomethyl-2-propoxy-phenol hydrochloride (109 mg, 0.50 mmole), 4 mL of N,N-dimethylformamide and triethylamine (75 μL, 0.54 mmole) is stirred for 15 minutes. Then (4-methoxymethylene-6-pyrrol-1-yl-4H-isoquinoline-1,3-dione (134 mg, 0.50 mmole) is added and the reaction mixture stirred for one hour. The reaction mixture is evaporated to dryness, taken up in 5% methanol in chloroform and passed through a short pad of Florisil eluting with 5% methanol in chloroform. The eluate is evaporated in vacuo and treated with acetonitrile, filtered and dried to give a beige solid, 94 mg, (45%), mp 215-216° C. dec; MS (ES+): m/z 418.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07713994B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-1002e16325fc4f38b7a7c03646426111 |
| Source note | uspto-grants-2010_05 |