HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(4-tert-Butylphenoxy)-N-{3-methoxy-4-[(methysulfonyl)amino]benzyl}acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(4-Tert-butylphenoxy)acetic acid | HCID 15718 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | N-[4-(aminomethyl)-3-methoxyphenyl]methanesulfonamide trifluoroacetic acid | HCID 69124640 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-tert-Butylphenoxy)-N-{3-methoxy-4-[(methysulfonyl)amino]benzyl}acetamide | HCID 21097472 | 43% |
Reaction Steps
A mixture of N-[4-(aminomethyl)-3-methoxyphenyl]methanesulfonamide trifluoroacetic acid (1.24 g, 3.6 mmol), (4-tert-butylphenoxy)acetic acid (625 mg, 3.0 mmol), 1-ethyl-3-(3′-dimethylaminopropyl) carbodiimide hydrogen chloride (EDC) (1.04 g, 5.4 mmol), triethylamine (1.21 g, 2.0 mmol) and 4-(dimethylamino)pyridine (DMAP) (110 mg, 0.9 mmol) in N,N-dimethylformamide (DMF) (30 ml) was treated in the same procedure described in Example 2(b) to give 543 mg (43% yield) of the title compound as a white amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07214824B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-09dd6a12c82847188d02a916c8bfa364 |
| Source note | uspto-grants-2007_05 |