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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101423Generated: October 30, 2026

Formaldehyde → HCID 68827109, compound

https://huagongshe.com/reaction/2101423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68826459HCID 68826459—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68827109HCID 6882710993%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572813B2
Source datasetuspto-grants-2009_08
ORD IDord-1d3a9bf998384e87955f1efeb29694eb
Source noteuspto-grants-2009_08