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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511629Generated: October 30, 2026

3-{[(2-amino-4-tert-butylphenyl)carbamoyl]methyl}-N-methoxy-N-methylcyclobutane-1-carboxamide → HCID 178502664, compound

https://huagongshe.com/reaction/511629

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-{[(2-amino-4-tert-butylphenyl)carbamoyl]methyl}-N-methoxy-N-methylcyclobutane-1-carboxamideHCID 86666122—
SolventAcetic AcidHCID 176—
ProductHCID 178502664HCID 178502664116.1%

Reaction Steps

A stirred solution of 3-{[(2-amino-4-tert-butylphenyl)carbamoyl]methyl}-N-methoxy-N-methylcyclobutane-1-carboxamide (70%, 2.62 g, 5.28 mmol) in acetic acid (25 ml) was heated to reflux for 1 h. The reaction mixture was concentrated under reduced pressure, and the residue partitioned between sat. NaHCO3 (aq) (25 ml) and EtOAc (25 ml), and the layers separated. The aqueous layer was extracted with EtOAc (2×25 ml), the combined organics were washed with brine (50 ml), dried (MgSO4) and concentrated. The crude material was purified by silica flash column chromatography, eluting with 1-10% 2M NH3 in MeOH in DCM to afford the title compound (2.02 g, 93%) as a yellow gum: MS (ESI+) for C19H27N3O2 m/z 330.5 [M+H]+; LC purity 80% (UV), 100% (ELS), (ret. time, 1.51 min); 1H NMR (500 MHz, CHLOROFORM-d) δH ppm 7.56 (br. s., 1H), 7.48 (d, J=8.5 Hz, 1H), 7.30 (dd, J=8.5, 1.7 Hz, 1H), 3.80-3.90 (m, 1H), 3.65 (s, 3H), 3.47-3.57 (m, 1H), 3.20 (s, 3H), 2.94-3.13 (m, 2H), 2.88 (dt, J=16.1, 8.1 Hz, 1H), 2.32-2.60 (m, 2H), 2.01-2.17 (m, 2H), 1.38 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096634B2
Source datasetuspto-grants-2015_08
ORD IDord-e58fea016af54770b1f4f9ad7fe97d4a
Source noteuspto-grants-2015_08