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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923568Generated: October 31, 2026

Triethylamine → HCID 178490478, compound

https://huagongshe.com/reaction/923568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactanttert-butyl 2-(N-(4-cyanobenzyl)-4-(2-(4-methoxy-2-(trifluoromethyl)phenyl)acetamido)benzamido)acetateHCID 71076634—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178490478HCID 17849047844%

Reaction Steps

Prepared using General Procedure 19: To a stirring solution of tert-butyl 2-(N-(4-cyanobenzyl)-4-(2-(4-methoxy-2-(trifluoromethyl)phenyl)acetamido)benzamido)acetate INT-32 (229 mg, 0.394 mmol) in DMF (3 mL) were added triethylamine (142 μl, 0.984 mmol) and hydroxylamine hydrochloride (68.4 mg, 0.984 mmol). After stirring at room temperature for 72 h, the reaction mixture was diluted with water (50 mL) and extracted with DCM (3×20 mL). The organics were dried over MgSO4 and evaporated. The crude product was purified by column chromatography (MeOH/DCM) to yield 107 mg (44%) of tert-butyl 2-(N-(4-(N-hydroxycarbamimidoyl)benzyl)-4-(2-(4-methoxy-2-(trifluoromethyl)phenyl)acetamido)benzamido)acetate INT-33. LCMS-ESI (m/z) calculated for C31H33F3N4O6: 614; found 615 [M+H]+, tR=1.70 min (Method 10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278910B2
Source datasetuspto-grants-2016_03
ORD IDord-2a0ac798b75043368fb9b4e12120f72c
Source noteuspto-grants-2016_03