HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Bromide → HCID 70008567, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 69702214 | HCID 69702214 | — |
| Reactant | HCID 86758924 | HCID 86758924 | — |
| Product | HCID 70008567 | HCID 70008567 | — |
Reaction Steps
The product was prepared from 1-(4-piperidin-4-yl-phenyl)-8,9-dihydro-7H-2,7,9a-triaza-benzo[cd]azulen-6-one (Example 137) following the procedure for Example 132 a white solid (77%): mp >240° C. (dec); Rf=0.21 (10% methanolic ammonia/CHCl3); IR (KBr) 1662, 1473, 1379, 1304 cm−1; 1H NMR (DMSO-d6) δ 1.69-1.81 (m, 4H), 2.00-2.07 (m, 2H), 2.23 (s, 3H), 2.53-2.58 (m, 1H), 2.89-2.93 (m, 2H), 3.51-3.52 (m, 2H), 4.45-4.47 (m, 2H), 7.34 (t, 1H, J=7.8 Hz), 7.45 (d, 2H, J=8.2 Hz), 7.79 (d, 2H, J=8.3 Hz), 7.84-7.90 (m, 2H), 8.44 (t, 1H, J=5.6 Hz). HRMS calcd for C22H24N4O 360.1950 (M+), found 360.1944. Anal. (C22H24N4O.0.25H2O) C, H, N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06548494B1 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-c6b2aa324d764bdf91c2a7b1af3c58b5 |
| Source note | uspto-grants-2003_04 |