HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 4-tert-Butyl-N-[4-chloro-2-(hydroxy-pyridin-4-yl-methyl)-phenyl]-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-tert-butyl-N-(4-chloro-2-isonicotinoylphenyl)benzenesulfonamide | HCID 9823937 | — |
| Product | 4-tert-Butyl-N-[4-chloro-2-(hydroxy-pyridin-4-yl-methyl)-phenyl]-benzenesulfonamide | HCID 58646038 | — |
Reaction Steps
The title compound was prepared by the reduction of 4-tert-Butyl-N-[4-chloro-2-(pyridine-4-carbonyl)-phenyl]-benzenesulfonamide with NaBH4 according to the procedure described in the preceding example. MS: (M+H)=431.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07932252B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-ef95b760d6db4cdebf0882c3a23ede56 |
| Source note | uspto-grants-2011_04 |