HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Dimethylamino)ethanol → 2-(2-chloropyrimidin-5-yloxy)-N,N-dimethylethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Dimethylamino)ethanol | HCID 7902 | — |
| Reactant | 2-Chloro-5-pyrimidinol | HCID 14595700 | — |
| Reactant | tert-butyl 5-amino-4-cyano-3-(4-hydroxyphenyl)-1H-pyrazole-1-carboxylate | HCID 136027725 | — |
| Product | 2-(2-chloropyrimidin-5-yloxy)-N,N-dimethylethanamine | HCID 59447495 | — |
Reaction Steps
Compound 112B was prepared in a similar manner to the synthesis of step 1 of Example 35 by substituting compound 34D and compound 31F with 2-(dimethylamino)ethanol and compound 112A, respectively: ESI (+)MS: 201 (M+H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08232273B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-a1eb909c926f4edcaf8e0c36d7162c66 |
| Source note | uspto-grants-2012_07 |