HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → HCID 21934606, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 21934656 | HCID 21934656 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21934606 | HCID 21934606 | — |
Reaction Steps
To a round bottomed flask were added 50 mg of (2,6-dimethyl-pyrimidin-4-yl)-thiazol-2-yl-amine (23-2), chloroform (3.0 mL) and 47 mg of N-bromosuccinimide. The reaction was allowed to stir at room temperature for 2 hours. The chloroform was diluted with ethyl acetate and washed with saturated sodium bisulfite solution. The ethyl acetate was dried (MgSO4) and the solvent removed under high vac to give the desired product. The title compound was used as is. 1H-NMR (400 MHz, DMSO-d6) 11.05 (1H, s), 7.53 (1H, s), 6.69 (1H, d), 6.69 (1H, s), 2.54 (3H, s), 2.35 (3H, s). MS(M+1)=285.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115597B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-0df1f55ec8d84d75ad3fea24d8508298 |
| Source note | uspto-grants-2006_10 |