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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444874Generated: October 27, 2026

tert-butyl N-(4-methyl-1,3-thiazol-2-yl)carbamate → Tert-butyl 5-(2-(2-cyanopropan-2-yl)pyridin-4-yl)-4-methylthiazol-2-ylcarbamate

https://huagongshe.com/reaction/444874

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(4-methyl-1,3-thiazol-2-yl)carbamateHCID 45117839—
Reactant2-(4-Iodopyridin-2-yl)-2-methylpropanenitrileHCID 59293717—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 5-(2-(2-cyanopropan-2-yl)pyridin-4-yl)-4-methylthiazol-2-ylcarbamateHCID 59293723—

Reaction Conditions

Temperature100 °C

Reaction Steps

The title compound is prepared in analogy to the procedure described in Step 1.3, but using 2-(4-iodo-pyridin-2-yl)-2-methyl-propionitrile (Step 21.5) and (4-methyl-thiazol-2-yl)-carbamic acid tert-butyl ester (Step 18.4). The reaction mixture is stirred for 3 h at 100° C. Title compound: ESI-MS: 359.1 [M+H]+; TLC: Rf=0.47 (Hex/EtOAc, 1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476268B2
Source datasetuspto-grants-2013_07
ORD IDord-d6916f8695cb47b785e052b8ce215726
Source noteuspto-grants-2013_07