HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyloxyamine hydrochloride → HCID 178461277, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyloxyamine hydrochloride | HCID 102312 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 178461279 | HCID 178461279 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | HCID 178461277 | HCID 178461277 | 54.5% |
Reaction Steps
To a solution of 3-[(trans-4-hydroxy-cyclohexyl)-(trans-4-methyl-cyclohexanecarbonyl)-amino]-5-(4-oxo-cyclohex-1-enyl)-thiophene-2-carboxylic acid (30 mg, 0.065 mmol) in a 2:1 H2O-ethanol mixture (3 mL) were added O-benzylhydroxylamine hydrochloride (21 mg, 0.13 mmol) and sodium acetate (18 mg, 0.13 mmol), and the mixture was stirred at room temperature overnight. Then the mixture was extracted with CH2Cl2, organic phase was dried over Na2SO4, concentrated under reduced pressure, and purified by column chromatography on silica gel eluting with 2-15% MeOH in CH2Cl2 to give 20 mg (54%) of 5-{4-benzyloxyimino-cyclohex-1-enyl}-3-[(trans-4-hydroxy-cyclohexyl)-(trans-4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08158675B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-15d2c8446b594a7e9d0e671f640e8e1a |
| Source note | uspto-grants-2012_04 |