HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Disulfide → HCID 14518047, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | HCID 14518046 | HCID 14518046 | — |
| Reactant | HCID 20037933 | HCID 20037933 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14518047 | HCID 14518047 | 89% |
| Product | HCID 20037933 | HCID 20037933 | — |
Reaction Steps
To a stirred and cooled (-10° C.) mixture of 20.8 parts of carbon disulfide, 9 parts of N,N-methanetetraylbis[cyclohexanamine] and 135 parts of tetrahydrofuran was added dropwise a solution of 15 parts of 4-[[1-(phenylmethyl)-1H-benzimidazol-2-yl]methyl]-1-piperidineethanamine in tetrahyrofuran at a temperature below -10° C. The reaction mixture was allowed to reach room temperature and the solvent was evaporated. The residue was crystallized from acetonitrile. The precipitate was filtered off and the filtrate was evaporated, yielding 15 parts (89%) of 2-[[1-(2-isothiocyanatoethyl)-4-piperidinyl]methyl]-1-(phenylmethyl)-1H-benzimidazole (385).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04695575 |
| Source dataset | uspto-grants-1987_09 |
| ORD ID | ord-ccb53dc6f387421696241d9d55b65e44 |
| Source note | uspto-grants-1987_09 |