HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 178466762, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzene, 1-ethoxy-4-isocyanato- | HCID 122887 | — |
| Reactant | HCID 178512242 | HCID 178512242 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178466762 | HCID 178466762 | 85% |
Reaction Steps
N-(4-Amino-benzyl)-N′-cyano-N″-quinolin-5-yl-guanidine (100 mg, 0.380 mmol) and 1-ethoxy-4-isocyanato-benzene (61 mg,, 0.39 mmol) were dissolved in and mixture of N,N-dimethylformamide (2.0 mL).and tetrahydrofuran (1.0 mL). Triethylamine (0.060 mL, 0.390 mmol) was added. The reaction mixture was shaken at room temperature for 12 hours. The solvent was removed in vacuo to give the title compound (yield=85%). 1H NMR (DMSO-d6, ppm): 8.34 (br, s, 2H); 7.41-7.21 (m, 10H); 6.82-6.76 (m, 2H); 4.43 (s, 2H); 3.93 (dq, 2H); 1.28 (dt, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06255323B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-53a6d362362245f4902ab32638a00d79 |
| Source note | uspto-grants-2001_07 |