HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 58825057, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 15957952 | HCID 15957952 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58825057 | HCID 58825057 | 11.9% |
Reaction Steps
To an ice cold solution of 50 mg (0.113 mmol) of 6-(4-benzyloxy-phenyl)-7-cyclohexyl-pyrazolo[1,5-a]pyrimidine-2-carboxylic acid methyl ester in 2 mL of dichloromethane (DCM) was added a solution of 21 mg (0.118 mmol) of N-bromosuccinimide (NBS) in 1 mL of DCM and the resulting mixture was allowed to warm up to rt and stirred at rt overnight. The reaction mixture was concentrated to give a residue which was chromatographed on silica gel (5% ethyl acetate in dichloromethane) to afford 7 mg (11% yield) of 6-(4-benzyloxy-phenyl)-3-bromo-7-cyclohexyl-pyrazolo[1,5-a]pyrimidine-2-carboxylic acid methyl ester as a colorless oil as indicated by 1H NMR (90% purity); LC-MS—calcd for C27H26BrN3O3 [M++H]+: 520.12, found: 520.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07196111B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-8fcab269901a484c96a194bd0fabbbc4 |
| Source note | uspto-grants-2007_03 |