HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Azidomethyl)furan → HCID 178479136, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Azidomethyl)furan | HCID 23315798 | — |
| Reactant | 4-Pent-4-ynyl-1H-imidazol-2-ylamine hydrochloride | HCID 178442251 | — |
| Product | HCID 178479136 | HCID 178479136 | 50% |
Reaction Steps
4-Pent-4-ynyl-1H-imidazol-2-ylamine hydrochloride (0.093 g, 0.500 mmol) was reacted with 2-azidomethyl-furan (0.074 g, 0.601 mmol) following the general procedure for click reactions outlined above to produce 4-[3-(1-Furan-2-ylmethyl-1H-[1,2,3]triazol-4-yl)-propyl]-1Himidazol-2-ylamine hydrochloride (0.075, 50%) as a pale yellow solid. 1H NMR (300 MHz, DMSO) δ 7.85 (s, 1H), δ 7.65 (s, 1H), δ 6.70 (s, 2H), δ 6.64 (s, 1H), δ 6.52 (t, 1H), δ 6.46 (s, 1H), δ 5.58 (s, 2H), δ 2.61 (t, 2H), δ 2.41 (t, 21-1), δ 1.82 (m, 2H) ppm; 13C NMR (75 MHz, DMSO) δ 163.6, 149.4, 147.9, 147.4, 144.3, 128.5, 122.6, 111.5, 110.3, 109.9, 46.3, 28.4, 24.9 ppm; HRMS (ESI) calcd for C13H16N6O (M+) 272.1458, found 272.1460.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367713B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-a64c3df9e5ed4af681e9fc9d5733b33d |
| Source note | uspto-grants-2013_02 |