HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → Trifluoroacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86636772 | HCID 86636772 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 44548946 | HCID 44548946 | — |
Reaction Steps
1-(4-(4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-(4-oxopiperidin-1-yl)-1,3,5-triazin-2-yl)phenyl)-3-(pyridin-4-yl)urea-TFA (56 mg) was taken up in methanol/tetrahydrofuran (1:1, 6 mL), and the mixture at 0° C. was treated with sodium borohydride (10 mg). After warming to room temperature, the mixture was concentrated to a residue which then was purified by HPLC to give the title compound as its TFA salt.; MS (ES+) 503.0 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09174963B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-d61331c0ec554042a9876663fde55c67 |
| Source note | uspto-grants-2015_11 |