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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-{[(2-amino-4-tert-butylphenyl)carbamoyl]methyl}-N-methoxy-N-methylcyclobutane-1-carboxamide | HCID 86666122 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178502664 | HCID 178502664 | 116.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096634B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-e58fea016af54770b1f4f9ad7fe97d4a |
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| Source note | uspto-grants-2015_08 |
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