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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516220Generated: October 27, 2026

Sulfuric Acid → 1-[4-(2-Amino-4-methyl-thiazol-5-yl)-pyridin-2-yl]-cyclobutanecarboxylic acid amide

https://huagongshe.com/reaction/1516220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant{5-[2-(1-Cyano-cyclobutyl)-pyridin-4-yl]-4-methyl-thiazol-2-yl}-carbamic acid tert-butyl esterHCID 59293719—
Product1-[4-(2-Amino-4-methyl-thiazol-5-yl)-pyridin-2-yl]-cyclobutanecarboxylic acid amideHCID 59293688—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of {5-[2-(1-cyano-cyclobutyl)-pyridin-4-yl]-4-methyl-thiazol-2-yl}-carbamic acid tert-butyl ester (Step 19.2) (640 mg, 1.73 mmol) and concentrated sulfuric acid is stirred for 40 min at 0° C., allowed to warm to rt, stirred for 1 h, quenched by addition of a saturated solution of NaHCO3 (50 mL) and extracted with DCM (3×75 mL). The organic phase is washed with a saturated solution of NaHCO3 (2×50 mL), dried (Na2SO4), filtered and concentrated. The residue is purified by silica gel column chromatography (DCM/MeOH/NH3aq, 99:0:1→93:6:1) to afford 35 mg of the title compound as a yellow solid: ESI-MS: 289.1 [M+H]+; TLC: Rf=0.32 (DCM/MeOH, 9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08227462B2
Source datasetuspto-grants-2012_07
ORD IDord-d333d4db62294919828656f7f0df25a4
Source noteuspto-grants-2012_07