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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226301Generated: October 29, 2026

Sulfuric acid magnesium salt (1:1) → (6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}-5-chloro-3-pyridyl)methanol

https://huagongshe.com/reaction/226301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantPotassium sodium tartarateHCID 9855836—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactantethyl 6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}-5-chloronicotinateHCID 68967686—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
Product(6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}-5-chloro-3-pyridyl)methanolHCID 6896285845%

Reaction Steps

A diisobutylaluminum hydride in toluene solution (15.7 ml) was dropwise added to a solution of ethyl 6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}-5-chloronicotinate (4.7 g) in toluene (50 ml) with stirring at −30˜−50° C. under atmospheric pressure of nitrogen, and the reaction mixture was stirred at −20˜−40° C. for 2 hours. A MeOH (5 ml) was added to a reaction mixture at −40° C. and saturated sodium potassium tartrate aqueous solution (10 ml) and MgSO4 (10 g) and the resultant mixture was stirred at ambient temperature for 20 minutes. The reaction mixture was filtrated and the filtrate was dried over MgSO4. The solvent was evaporated in vacuo and the residue was chromatographed on silicagel eluting with AcOEt-MeOH (9:1). The eluted fractions containing the desired product were collected and evaporated in vacuo to give (6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}-5-chloro-3-pyridyl)methanol (1.87 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557127B2
Source datasetuspto-grants-2009_07
ORD IDord-ab7104a7bb75428aac2771305ab8bbe2
Source noteuspto-grants-2009_07