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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109034Generated: October 26, 2026

Sodium Bicarbonate → HCID 178483849, compound

https://huagongshe.com/reaction/2109034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant1-Amino-3,3-diethoxypropaneHCID 521029—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl N-(3-oxopropyl)carbamateHCID 10910051—
ReactantHCID 178484811HCID 178484811—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
ProductHCID 178483849HCID 17848384989.1%

Reaction Steps

N-(5-Chloropyridin-2-yl)-3-({[trans-4-(methylamino)cyclohexyl]-carbonyl}amino)furo[3,2-b]pyridine-2-carboxamide trihydrochloride (300 mg) obtained in Example 119 is suspended in chloroform (7 ml). To the suspension are added 3-t-butoxycarbonylaminopropanal (208 mg), which can be prepared from 3-aminopropionaldehyde diethyl acetal in two steps according to the method described in a literature (Synthesis, 1994, 37) and triethylamine (334 μl) under ice-cooling, and the mixture is stirred for a few minutes. After addition of sodium triacetoxy borohydride (190 mg), the reaction solution is warmed to room temperature and stirred for 2 hours. To the reaction solution is poured saturated aqueous sodium hydrogen carbonate solution under ice-cooling, and the mixture is extracted with chloroform. The organic layer is washed successively with water and saturated brine, dried over sodium sulfate, and the solvent is evaporated under reduced pressure. The resulting residue is purified by NH-silica gel column chromatography (eluent: ethyl acetate followed by ethyl acetate/methanol=20/1) to give the title compound (291 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514449B2
Source datasetuspto-grants-2009_04
ORD IDord-f5df9299378c4a7bbcfc46a667e54714
Source noteuspto-grants-2009_04