HuagongsheHuagongshe Chemistry Print Report · For research reference only
phenyl 3-(1-methyl-1H-tetraazol-5-yl)phenylcarbamate → HCID 44447136, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | phenyl 3-(1-methyl-1H-tetraazol-5-yl)phenylcarbamate | HCID 22252681 | — |
| Reactant | HCID 58997665 | HCID 58997665 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 44447136 | HCID 44447136 | 78.5% |
Reaction Steps
The product of Step g (50 mg, 0.19 mmol, 1 eq.), phenyl 3-(1-methyl-1H-tetraazol-5-yl)phenylcarbamate (55 mg, 0.19 mmol, 1 eq.) and acetonitrile (3 mL) were mixed at 25° C. under N2 overnight. Worked up by stripping off the solvents then purifying the residue over silica gel in 100% EtOAc to 4:1 EtOAc/MeOH. Obtained 70 mg of a white glass as product. NMR (300 MHz, CDCl3) δ 7.86 (s, 1H); 7.6 (d, 1H, J=7 Hz); 7.38 (t, 1H, J=7 Hz); 7.29 (d, 1H, J=7 Hz); 7.20-7.00 (m, 2H); 6.92 (t, 2H, J=7 Hz); 4.13 (s, 3H) 4.05-3.85 (m, 1H); 3.80-3.60(m, 1H); 2.80-2.40 (m, 8H); 1.85-1.60 (m, 2H); 1.18 (d, 3H, J=7 Hz); 1.00 (t, 3H, J=7 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07291744B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-a8e37679b068426dae28dab54e27d5e0 |
| Source note | uspto-grants-2007_11 |