Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509534Generated: October 26, 2026

Triethylamine → HCID 68493219, compound

https://huagongshe.com/reaction/509534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Amino-5-bromonicotinic acidHCID 737445—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactanttert-butyl N-[[4-(hydrazinecarbonyl)phenyl]methyl]-N-methyl-carbamateHCID 67425410—
SolventDimethylformamideHCID 6228—
SolventWater ethylacetateHCID 22728543—
ProductHCID 68493219HCID 6849321958%

Reaction Steps

2-amino-5-bromo-pyridine-3-carboxylic acid (776.9 mg, 3.580 mmol) and triethylamine (724.5 mg, 997.9 μL 7.160 mmol) were added to a stirred solution of tert-butyl N-[[4-(hydrazinecarbonyl)phenyl]methyl]-N-methyl-carbamate (1 g, 3.580 mmol in DMF (8 mL). To the stirred slurry was added TBTU (1.724 g, 5.370 mmol) and the mixture stirred at ambient for 60 hours. The mixture was diluted with EtOAc/water and the layers separated. The mixture was extracted with ethyl acetate (×3) and the combined extracts washed with saturated aqueous NaHCO3 (×1) and brine (×1), dried (MgSO4), filtered and concentrated in vacuo. The resultant residue was purified by column chromatography (ISCO Companion™, 12 g column, 0-100% EtOAc/Petroleum ether) and the product containing fractions concentrated in vacuo. The residue was triturated from acetonitrile to give the desired sub-title product as a cream solid (992 mg, 58% Yield). 1H NMR (400.0 MHz, DMSO) δ 1.39-1.45 (m, 9H), 2.80 (s, 3H), 4.45 (s, 2H), 7.28 (s, 2H), 7.35 (d, J=8.2 Hz, 2H), 7.90 (d, J=7.8 Hz, 2H), 8.20 (d, J=2.4 Hz, 1H), 8.24 (d, J=2.2 Hz, 1H), 10.50 (s, 1H) and 10.54 (s, 1H) ppm; MS (ES+) 480.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096584B2
Source datasetuspto-grants-2015_08
ORD IDord-27019ec841394748859afddd9e731535
Source noteuspto-grants-2015_08