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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435408Generated: November 1, 2026

N-{5-(acetylamino)-2-[(tetrahydro-2H-pyran-4-ylmethyl)amino]phenyl}-2,2-dimethylpropanamide → N-[2-tert-Butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazol-5-yl]acetamide

https://huagongshe.com/reaction/1435408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-{5-(acetylamino)-2-[(tetrahydro-2H-pyran-4-ylmethyl)amino]phenyl}-2,2-dimethylpropanamideHCID 57937309—
SolventAcetic AcidHCID 176—
ProductN-[2-tert-Butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazol-5-yl]acetamideHCID 57937300—

Reaction Conditions

Temperature120 °C

Reaction Steps

N-{5-(acetylamino)-2-[(tetrahydro-2H-pyran-4-ylmethyl)amino]phenyl}-2,2-dimethylpropanamide (33.1 g, 95.3 mmol) was dissolved in AcOH (250 mL). The solution was heated at 120° C. for 8 h. Upon evaporation of the solvent, the residue was dissolved in EtOAc (500 mL), washed with 2N NaOH (3×50 mL), brine (50 mL) and dried over anhydrous Na2SO4. The crude product was recrystallized from EtOAc. Yield: 29.0 g (92%). 1H NMR (400 MHz, CHLOROFORM-D): δ 1.48-1.54 (m, 4 H), 1.56 (s, 9 H), 2.20 (s, 3 H), 2.24-2.35 (m, 1 H), 3.28-3.35 (m, 2 H), 3.96 (t, J=2.83 Hz, 1 H), 3.99 (t, J=3.03 Hz, 1 H), 4.19 (d, J=7.42 Hz, 2H), 7.27 (d, J=8.59 Hz, 1 H), 7.34 (br.s, 1 H), 7.57 (dd, J=8.79, 1.95 Hz, 1 H), 7.67 (d, J=1.95 Hz, 1 H); MS (ESI) (M+H)+=330.04.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615642B2
Source datasetuspto-grants-2009_11
ORD IDord-aa911cdf35b34a55a5bd5db891ab510e
Source noteuspto-grants-2009_11