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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868286Generated: October 31, 2026

Sodium borohydride → 6-Bis(phenylmethyl)amino-4,5-diamino-pyridine-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1868286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-Amino-6-bis(phenylmethyl)amino-5-nitro-pyridine-3-carboxylic acid ethyl esterHCID 69064703—
CatalystNickel chloride hydrateHCID 16212333—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product6-Bis(phenylmethyl)amino-4,5-diamino-pyridine-3-carboxylic acid ethyl esterHCID 6907047424.1%

Reaction Steps

Sodium borohydride (151 mg, 4.1 mmol) was added to a solution of nickel (II) chloride hydrate (261 mg, 1.1 mmol) in MeOH (26 mL). After 30 min. at room temperature, a solution of 4-amino-6-bis(phenylmethyl)amino-5-nitro-pyridine-3-carboxylic acid ethyl ester (0.9 g, 2.2 mmol) in dichloromethane (5 mL) was added followed by the addition of sodium borohydride (353 mg). The mixture was stirred over night then filtered through a layer of silica gel. The organic was diluted with dichloromethane, washed with brine and dried over sodium sulfate. The organics were filtered, concentrated and purified by column chromatography (dichloromethane:methanol, 20:1). 11 was obtained as a white solid (200 mg). 1H NMR (400 MHz, d6-DMSO) δ: 1.26 (t, J=7.1 Hz, 3H), 4.21 (s, 4H), 4.22 (q, J=7.1 Hz, 2H), 4.52 (s, 2H), 6.73 (s, 2H), 7.14-7.31 (m, 10H), 8.01 (s, 1H). ESIMS, M/Z, 377 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635695B2
Source datasetuspto-grants-2009_12
ORD IDord-c3255ef06e3f4b58834b3a729191b253
Source noteuspto-grants-2009_12