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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370372Generated: October 27, 2026

tert-butyl N-(4-methyl-1,3-thiazol-2-yl)carbamate → {5-[2-(1-Cyano-cyclobutyl)-pyridin-4-yl]-4-methyl-thiazol-2-yl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2370372

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(4-methyl-1,3-thiazol-2-yl)carbamateHCID 45117839—
Reactant1-(4-Bromopyridin-2-yl)cyclobutane-1-carbonitrileHCID 57417094—
SolventEthyl AcetateHCID 8857—
Product{5-[2-(1-Cyano-cyclobutyl)-pyridin-4-yl]-4-methyl-thiazol-2-yl}-carbamic acid tert-butyl esterHCID 59293719—

Reaction Conditions

Temperature100 °C

Reaction Steps

The title compound is prepared in analogy to the procedure described in Step 1.3, but using 1-(4-bromo-pyridin-2-yl)-cyclobutanecarbonitrile (Step 19.3) 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: 371.1 [M+H]+; tR=4.86 min (System 1); TLC: Rf=0.66 (Hex/EtOAc, 1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710085B2
Source datasetuspto-grants-2014_04
ORD IDord-3dc3af8587fd4259aa8b87290422ae80
Source noteuspto-grants-2014_04