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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169765Generated: November 4, 2026

(R)-2-(2-chloro-5-(2-thienyl)pyrimidine-4-ylamino)butan-1-ol → (S)-N-(ethoxycarbonyl)-S-(4-{[4-{[(R)-1-(hydroxymethyl)propyl]amino}-5-(2-thienyl)pyrimidine-2-yl]amino}phenyl)-S-cyclopropylsulfoximide

https://huagongshe.com/reaction/1169765

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-2-(2-chloro-5-(2-thienyl)pyrimidine-4-ylamino)butan-1-olHCID 58985648—
Reactant(S)-S-(4-aminophenyl)-N-(ethoxycarbonyl)-S-cyclo-propyl-sulfoximideHCID 59550868—
Product(S)-N-(ethoxycarbonyl)-S-(4-{[4-{[(R)-1-(hydroxymethyl)propyl]amino}-5-(2-thienyl)pyrimidine-2-yl]amino}phenyl)-S-cyclopropylsulfoximideHCID 5898579547%

Reaction Steps

In the reaction of (R)-2-(2-chloro-5-(2-thienyl)pyrimidine-4-ylamino)butan-1-ol (300 mg, 1.06 mmol) with (S)—S-(4-aminophenyl)-N-(ethoxycarbonyl)-S-cyclo-propyl-sulfoximide (258 mg, 0.96 mmol) according to procedure 5c, the desired product is obtained in 47% yield (256 mg) after chromatographic purification (silica gel, dichloromethane/ethanol (0%-20% ethanol)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825128B2
Source datasetuspto-grants-2010_11
ORD IDord-e84214322bd74c3098ed3d3273c4d75f
Source noteuspto-grants-2010_11