HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 66755273, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Triacetoxyborohydride | HCID 2724942 | — |
| Reactant | HCID 66754850 | HCID 66754850 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66755273 | HCID 66755273 | — |
Reaction Steps
A solution of 98.0 mg (0.17 mmol) 2-[6-chloro-3-(4-methoxybenzenesulfonyl)-2-oxo-2,3-dihydrobenzimidazol-1-yl]-2-phenyl-N-(2-piperazin-1-yl-ethyl)acetamide (Example 131) in 4 ml of THF was mixed with 5.54 mg (0.19 mmol) of paraformaldehyde and 170 mg of MP-triacetoxyborohydride resin (Argonaut, 2.55 mmol/g, 0.42 mmol) and shaken at room temperature overnight. The solid phase reagent was filtered off and washed with dichloromethane. The filtrate was concentrated under reduced pressure. The residue was purified by preparative RP-HPLC (mobile phase: gradient from 10% to 80% acetonitrile in water, 0.1% trifluoroacetic acid as modulator). Yield: 69.6 mg (69%) of colorless solid
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08791148B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-b8f1712521c84f379854b514055d6eca |
| Source note | uspto-grants-2014_07 |