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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169764Generated: October 29, 2026

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

https://huagongshe.com/reaction/1169764

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-2-(2-chloro-5-(2-thienyl)pyrimidine-4-ylamino)butan-1-olHCID 58985648—
Reactant(R)-S-(4-aminophenyl)-N-(ethoxycarbonyl)-S-cyclo-propyl-sulfoximideHCID 59550884—
Product(R)-N-(ethoxycarbonyl)-S-(4-{[4-{[(R)-1-(hydroxymethyl)propyl]amino}-5-(2-thienyl)pyrimidine-2-yl]amino}phenyl)-S-cyclopropylsulfoximideHCID 2476951540%

Reaction Steps

In the reaction of (R)-2-(2-chloro-5-(2-thienyl)pyrimidine-4-ylamino)butan-1-ol (270 mg, 0.95 mmol) with (R)—S-(4-aminophenyl)-N-(ethoxycarbonyl)-S-cyclo-propyl-sulfoximide (224 mg, 0.83 mmol) according to procedure 5c, the desired product is obtained in 40% yield (170 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-5423f61414b84fe7b37524ee34cf74d8
Source noteuspto-grants-2010_11