HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178453892, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Fluoro-3-(4-piperidinyl)-1,2-benzisoxazole | HCID 2794755 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 178453924 | HCID 178453924 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 178453892 | HCID 178453892 | 102% |
Reaction Steps
A mixture of 5-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (1.3 g, 5 mmol), trans-[4-(2-oxo-ethyl)-cyclohexyl]-carbamic acid tert-butyl ester (example 1, intermediate C) (1.6 g, 6 mmol), triethylamine (0.64 mL, 5 mmol) in 1,2 dichloroethane (27 mL) was stirred for 4 h at room temperature and sodium triacetoxyborohydride (1.9 g, 9 mmol) was added slowly and the resulting solution was stirred for 12 hours until the TLC indicated completion of the reaction. The mixture was filtrated and concentrated to dryness and purified with column chromatography on silica gel using CH2Cl2—CH2Cl2/MeOH (1-9:1). The product fractions were concentrated to give 2.3 g (5.1 mmol, 100% yield) of a off-white solid. MS (m/e): 446.3 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829029B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-376f96ff0f514fed88ddc6e5c17bd469 |
| Source note | uspto-grants-2014_09 |