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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783896Generated: October 30, 2026

2,2-Dimethylbutyryl chloride → HCID 57591005, compound

https://huagongshe.com/reaction/1783896

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Dimethylbutyryl chlorideHCID 79958—
ReactantHCID 68861536HCID 68861536—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 57591005HCID 5759100587%

Reaction Steps

2,2-Dimethylbutyryl chloride (24.6 mg, 0.18 mmol) was added to a mixture of 1-(cyclohexylmethyl)-2-(1,1-dimethylpropyl)-1H-benzimidazol-5-amine hydrochloride (65.0 mg, 0.15 mmol) (for preparation see in Example 7, step B) and DMAP (73.3 mg, 0.60 mmol) in acetonitrile (5 mL) at 0° C. The mixture was stirred for 6 h at room temperature, diluted with EtOAc (50 mL), washed with saturated NaHCO3 aqueous solution (10 mL), saturated NaCl aqueous solution (10 mL) and dried over Na2SO4. After filtration and evaporation, the residue was purified by MPLC (EtOAc as eluent on silica gel) to give the desired title compound as a syrup (51.6 mg, 87%). 1H NMR (400 MHz, CD3OD): δ 0.84 (t, J=7.52 Hz, 3H), 0.91 (t, J=7.52 Hz, 3H), 1.25 (m, 5H), 1.28 (s, 6H), 1.64 (m, 3H), 1.67 (s, 6H), 1.72 (q, J=7.49 Hz, 2H), 1.78 (m, 2H), 2.02 (q, J=7.49 Hz, 2H), 2.13 (m, 1H), 4.45 (d, J=7.62 Hz, 2H), 7.64 (dd, J=8.98, 1.76 Hz, 1H), 7.85 (d, J=9.18 Hz, 1H), 8.34 (s, 1H). MS (ESI) (M+H)+: 398.3. Anal. Calcd for C25H39N3O+1.50 TFA+0.70H2O (581.25): C, 57.86; H, 7.27; N, 7.23. Found: C, 57.90; H, 7.19; N, 7.34.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501447B2
Source datasetuspto-grants-2009_03
ORD IDord-aba0c9350b3d445eba5866611aea8a27
Source noteuspto-grants-2009_03