HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Disulfide → HCID 178480613, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | 4-Fluoro-5-(4-methylpiperazin-1-yl)benzene-1,2-diamine | HCID 10656760 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178480613 | HCID 178480613 | 94% |
Reaction Steps
6-Fluoro-5-(4-methylpiperazin-1-yl)-2-mercapto-1H-benzimidazole (15.0 g, 94%) was prepared by a similar procedure to that described in preparation 1 (step 5) using the diamine (14.0 g, 0.06 mol) (obtained in step 3 above), carbon disulfide (6.1 g, 0.08 mol), potassium hydroxide (4.49 g, 0.08 mol), ethanol (70 mL) and water (10 mL). mp 290° C. (decomp.); IR (KBr) 3088, 1481 cm-1 ; 1H NMR (DMSO-d6) δ 2.24 (s, 3H, CH3), 2.50 (t, J=4.3 Hz, 4H, N(CH2)2), 3.00 (t, J=4.4 Hz, 4H, N(CH2)2), 6.78 (d, J=7.3 Hz, 1H), 7.00 (d, J=11.9 Hz, 1H); Mass (m/z) 266 (M+.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06051570 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-7d3803438e01451fa13f218ec26fc475 |
| Source note | uspto-grants-2000_04 |