HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → HCID 14518102, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | N-[1-(2-aminoethyl)-4-piperidinyl]-1-(4-fluorophenylmethyl)-1H-benzimidazol-2-amine | HCID 12891741 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14518102 | HCID 14518102 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a stirred mixture of 5.3 parts of cyanogen bromide, 106. parts of anhydrous sodium carbonate and 45 parts of tetrahydrofuran was added dropwise a solution of 18.35 parts of N-[1-(2-aminoethyl)-4-piperidinyl]-1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-amine in tetrahydrofuran at a temperature between -10° C. and -20° C. Upon completion, stirring was continued for 2 hours at -10° C. After heating to 0° C., the whole was filtered and the filtrate was evaporated, yielding 19 parts (100%) of [2[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinyl]ethyl]cyanimide as a residue (187).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04634704 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-a99a6b3da8fd4de0a9b402070e2fc7a2 |
| Source note | uspto-grants-1987_01 |