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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362111Generated: October 25, 2026

Triethylamine → 5-Bromo-3-[(3-morpholin-4-yl-propylamino)methyl]pyridin-2-ylamine

https://huagongshe.com/reaction/1362111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-(3-Aminopropyl)morpholineHCID 61055—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Amino-5-bromonicotinaldehyde hydrobromideHCID 86606146—
SolventMethanolHCID 887—
Product5-Bromo-3-[(3-morpholin-4-yl-propylamino)methyl]pyridin-2-ylamineHCID 5945694754%

Reaction Steps

To a solution of 2-amino-5-bromo-pyridine-3-carbaldehyde hydrobromide (4.30 g, 15.3 mmol) in MeOH (100 mL) was added triethylamine (4.3 mL, 31 mmol) and the mixture was stirred at room temperature for 10 min. The resulting suspension was treated with 4-(3-aminopropyl)morpholine (2.5 mL, 17 mmol) and the mixture was stirred for 7 h. TLC analysis indicated remaining starting material. Additional 4-(3-aminopropyl)morpholine (1.0 mL, 6.8 mmol) was added, and the mixture was allowed to stir overnight at room temperature. The mixture was cooled and then NaBH4 (0.87 g, 23.0 mmol) was added in two portions. The mixture was stirred at room temperature for 4 h. The solvent was removed in vacuo. Purification by column chromatography (silica gel, CH2Cl2/MeOH/Et3N, 97/2.5/0.5 to 85/14.5/0.5) gave the title compound (2.70 g, 54%) as a brown oil: MS (ESI) m/e 329 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-1631858270a5415c8ff9059ae98f209b
Source noteuspto-grants-2011_02