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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661121Generated: November 2, 2026

Dimethylformamide → HCID 86613780, compound

https://huagongshe.com/reaction/661121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantLithium ChlorideHCID 433294—
Reactanttert-butyl N-(5-(tributylstannyl)-1,3-thiazol-2-yl)carbamateHCID 2763269—
Reactant7-bromoquinazolineHCID 11195146—
CatalystHCID 178418397HCID 178418397—
ProductHCID 86613780HCID 8661378046.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred mixture of flame-dried LiCl (45 mg, 1052 μmol), 7-bromoquinazoline (22 mg, 105 μmol), and Pd(Ph3P)4 (6.1 mg, 5.3 μmol), was added a solution of tert-butyl 5-(tributylstannyl)thiazol-2-ylcarbamate (77 mg, 158 μmol) in DMF (1.50 mL, 19372 μmol). The resulting mixture was stirred at 80° C. overnight. The mixture was concentrated, and the crude residue was dissolved in DCM and mixed with SiO2. The solvent was evaporated, and the residue was purified with flash column chromatography (pure DCM→5% MeOH in DCM) followed by washing with ether to obtain the desired product tert-butyl 5-(quinazolin-7-yl)thiazol-2-ylcarbamate (16 mg, 46%) as a pale yellow solid. LCMS (API-ES) m/z (%): 329.4 (100%, M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084479B2
Source datasetuspto-grants-2011_12
ORD IDord-5875b55c07084e35966648a4f76f5e3e
Source noteuspto-grants-2011_12