HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 68827109, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 68826459 | HCID 68826459 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68827109 | HCID 68827109 | 93% |
Reaction Steps
The title benzamide from Example 1 (21 mg) was dissolved in THF prior to the addition of Hunigs's base (0.01 mL). Next, 37% formaldehyde (0.017 mL) was added along with 4A molecular sieves. After 3 h, NaHB(OAc)3 (38 mg) was added. This mixture was stirred an additional 2 h before the reaction was quenched-with NaHCO3 solution. This was extracted with EtOAc. The EtOAc was dried and concentrated. Reverse phase HPLC purification (gradient elution, water/acetonitrile/TFA) of the resulting residue provided the title benzamide N-[2-[[(1S,2S)-2-[(4-chlorobenzyl)(methyl)amino]cyclohexyl]amino]-2-oxoethyl]-3-(trifluoromethyl)benzamide (10 mg). MS found: (M+H)+=482.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07572813B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-1d3a9bf998384e87955f1efeb29694eb |
| Source note | uspto-grants-2009_08 |