HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 178527806, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | 4-(Piperazin-1-yl)benzene-1,2-diamine | HCID 13354067 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178527806 | HCID 178527806 | 85% |
Reaction Steps
5-(Piperazin-1-yl)-2-mercapto-1H-benzimidazole (7.9 g, 85%) was prepared by an analogous procedure to that described in preparation 1 (step 5) using the diamine (8.0 g, 0.04 mol) (obtained in step 2 above), carbon disulfide (3.6 g, 0.048 mol), ethanol (40 nmL) and water (4 nmL). mp 260-261° C.; IR (KBr) 3350, 1498 cm-1 ; 1H NMR (DMSO-d6) δ 2.40 (s, 1H, SH), 3.00 (t, J=4.4 Hz, 4H, N(CH2)2), 3.50 (brs, 1H, NH), 4.42 (t, J=4.5 Hz, 4H, N(CH2)2), 6.68 (s, 1H), 6.85 (d, J=8.0 Hz, 1H), 7.03 (d, J=8.4 Hz, 1H) ; Mass (m/z) 234 (M+.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06051570 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-a78a1eca757b4423b2ec5a5f115beab6 |
| Source note | uspto-grants-2000_04 |