HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dichloroquinazoline → HCID 178478401, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichloroquinazoline | HCID 252886 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | (4-(2-(1H-1,2,3,4-tetrazol-5-yl)phenyl)phenyl)methanamine hydrochloride | HCID 178479176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178478401 | HCID 178478401 | 37.5% |
Reaction Steps
To 50 mL of tetrahydrofuran were added 2,4-dichloroquinazoline (0.30 g). N-[[-2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl amine hydrochloride (0.434 g) and 2.0 g of sodium acetate. The resulting suspension was stirred at room temperature for 53 hours at which time all the THF was removed by evaporation. The residue was purified by silica gel chromatography to yield 0.234 g of the desired product. (38%). The product was characterized as its sodium salt: 1H NMR (DMSO-d6, 400 MHz) δ9.30 (t, J=5.9 Hz, 1H), 8.31 (d, J=7.8 Hz, 1H), 7.79 (m, 1H), 7.61 (d, J=8.4 Hz, 1H), 7.52 (m, 2H), 7.32 (m, 3H), 7.18 (d, J=8.2 Hz, 2H), 7.07 (d, J=8.2 Hz, 2H), 4.72 (d, J=5.8 Hz, 2H); negative FAB MS m/e 412 (M-Na)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05187168 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-06427182d14c4c92a4d4defbd195c8cb |
| Source note | uspto-grants-1993_02 |