HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Isocyanatomethyl)thiophene → HCID 44128465, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Isocyanatomethyl)thiophene | HCID 15890621 | — |
| Reactant | 4-Diazo-4H-imidazole-5-carboxamide | HCID 53426585 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 44128465 | HCID 44128465 | — |
Reaction Steps
Thiophen-2-ylmethyl isocyanate (0.350 g, 2.5 mmol) was added drop wise to a suspension of 5-diazoimidazole-4-carboxamide (0.314 g, 2.3 mmol) in dry dimethylsulfoxide (2.5 mL) at room temperature under nitrogen. The resulting mixture was stirred at room temperature overnight. The reaction was quenched by the addition of ice and the solid product (off-white) was removed by filtration, washed with water and ethyl acetate and air dried to give the title compound. Yield: 0.405 g, 64%. IR vmax/cm−1 3094, 1732, 1690, 1607. 1H NMR δH (DMSO-d6) 5.68 (2H, s, CH2Ar), 7.03 (1H, dd, J=5.1, 3.5, ArH), 7.25 (1H, dd, J=3.5, 1.0, ArH), 7.55 (1H, dd, J=5.1, 1.0, ArH), 7.71 (1H, br s, NH), 7.83 (1H, br s, NH), 8.85 (1H, s, 6-H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08450479B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-9dd34706b0924f5dba6837bd0f905e66 |
| Source note | uspto-grants-2013_05 |