HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 25057012, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 66902076 | HCID 66902076 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 25057012 | HCID 25057012 | 17% |
Reaction Steps
2.4 16.9 mg (0.160 mmol) of cyanogen bromide are added to a solution of 60 mg (0.141 mmol) of 2-[3-(2,6-dimethylphenylamino)-6-fluoro-imidazo[1,2-a]pyridin-2-yl]benzohydrazide hydrochloride and 29.4 mg (0.350 mmol) of sodium hydrogencarbonate in 10 ml of water, and the mixture is stirred at RT for 2 hours. The precipitated product is filtered off with suction, dried and purified by preparative thin-layer chromatography, giving 10 mg (17%) of {2-[2-(5-amino-1,3,4-oxadiazol-2-yl)phenyl]-6-fluoroimidazo[1,2-a]pyridin-3-yl}-(2,6-dimethylphenyl)amine (“B1”) as solid; MS-FAB (M+H+)=415.8; Rf (HPLC, polar method): 1.07 min.;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153649B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-ac916e067cdf43debf268ea5bc5f50ba |
| Source note | uspto-grants-2012_04 |