HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 44331444, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | (R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamide | HCID 12047933 | — |
| Reactant | HCID 18678592 | HCID 18678592 | — |
| Product | HCID 44331444 | HCID 44331444 | 29.3% |
Reaction Steps
The title compound was prepared from N-[5-(2-amino-1-{R}-hydroxyethyl)-2-hydroxyphenyl]-methanesulfonamide (0.154 g, 0.63 mmol), 1-(2,5-difluoro-benzyl)-3-[4-(4-formyl-piperidine-1-sulfonyl)-phenyl]-1-isopropyl-urea (1.0 mmol), glacial acetic acid (0.036 g, 0.63 mmol) and sodium cyanoborohydride (0.039 g, 0.63 mmol) according to the general procedure used for example 84 (Step E) to give the final product (0.131 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06506901B2 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-5b46259cc9c24067bc48588cfe7c8da9 |
| Source note | uspto-grants-2003_01 |