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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350835Generated: October 31, 2026

Triethylamine → 2-(4-tert-Butylphenoxy)-N-{3-methoxy-4-[(methysulfonyl)amino]benzyl}acetamide

https://huagongshe.com/reaction/1350835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-(4-Tert-butylphenoxy)acetic acidHCID 15718—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN-[4-(aminomethyl)-3-methoxyphenyl]methanesulfonamide trifluoroacetic acidHCID 69124640—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
Product2-(4-tert-Butylphenoxy)-N-{3-methoxy-4-[(methysulfonyl)amino]benzyl}acetamideHCID 2109747243%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214824B2
Source datasetuspto-grants-2007_05
ORD IDord-09dd6a12c82847188d02a916c8bfa364
Source noteuspto-grants-2007_05