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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488805Generated: October 25, 2026

Diisopropylethylamine → tert-butyl N-[N-(5-propan-2-yl-1-quinolin-6-ylpyrazole-4-carbonyl)carbamimidoyl]carbamate

https://huagongshe.com/reaction/488805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant5-isopropyl-1-(6-quinolinyl)-1H-pyrazole-4-carboxylic acidHCID 22267640—
ReactantHCID 178454308HCID 178454308—
SolventDimethylformamideHCID 6228—
Producttert-butyl N-[N-(5-propan-2-yl-1-quinolin-6-ylpyrazole-4-carbonyl)carbamimidoyl]carbamateHCID 14101164822.5%

Reaction Steps

To a solution of 5-isopropyl-1-(6-quinolinyl)-1H-pyrazole-4-carboxylic acid (336.7 mg, 1.2 mmol) in 5 ml dimethylformamide was added N,N-diisopropylethylamine (0.42 ml, 2.39 mmol), benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (BOP reagent) (582 mg, 1.32 mmol) and tert-butoxycarbonylguanidine (210 mg, 1.32 mmol). The resulting solution was stirred at room temperature for 2 h, then heated to 60° C. for 2 h. The reaction mixture was then cooled to room temperature and concentrated to dryness in vacuo. The solid residue was partitioned between ethyl acetate and water. The ethyl acetate layer was washed with brine, dried (sodium sulfate) and concentrated to dryness in vacuo. The solid residue was triturated with methanol (1.5 ml), filtered, washed with diethyl ether and dried to yield the title compound as a white solid (114.3 mg, 22.5% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06974813B2
Source datasetuspto-grants-2005_12
ORD IDord-9fcc380d12e54b589c47d7110a0a176e
Source noteuspto-grants-2005_12