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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416201Generated: October 25, 2026

Hydrogen Sulfide → (4-[4-(2-Oxo-1,2-dihydro-quinolin-3-yl)-thiazol-2-yl]-phenyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2416201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
ReactantTert-butyl 4-cyanophenylcarbamateHCID 10130644—
Reactanttert-butyl N-(4-carbamothioylphenyl)carbamateHCID 22638585—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
Product(4-[4-(2-Oxo-1,2-dihydro-quinolin-3-yl)-thiazol-2-yl]-phenyl)-carbamic acid tert-butyl esterHCID 58810140—

Reaction Steps

A solution of 4-cyano-tert-butyloxycarbonylaniline (2.20 g, 10.0 mmol) in 20 mL of pyridine and 5 mL of TEA was purged with H2S gas for 7.0 h. Solvents were removed under vacuum. The resulting crude 4-Boc-aminobenzene-thiocarboxamide (yellow residue, 70% purity) was used directly in the next step. A solution of 4-Bocamino-benzenethiocarboxamide (205 mg, 70% pure, 0.57 mmol) and 3-(2-bromoacetyl)hydroquinolin-2-one (Example 27b, 78 mg, 0.29 mmol) in 50 mL of MeOH was heated at reflux for 4 h. After cooling to RT, the precipitates were collected by filtration to provide the title compound as an off-white solid. MS m/z: 420.2 (M+1). HRMS m/z: 420.1358 (M+H+, C23H21N3O3S Calc'd 420.1376).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06822097B1
Source datasetuspto-grants-2004_11
ORD IDord-a4d0dd2b38ca416c888d782c4b7407e0
Source noteuspto-grants-2004_11