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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2272969Erstellt: 25. Oktober 2026

Triethylamine → HCID 60491075, Verbindung

https://huagongshe.com/reaction/2272969

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Edukt1-tert-Butyl-1H-pyrazole-4-carboxylic acidHCID 24696291—
EduktHCID 178527226HCID 178527226—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 60491075HCID 60491075—

Reaktionsschritte

To a suspension of 5.00 g (29.7 mmol) 1-tert-butyl-1H-pyrazole-4-carboxylic acid and 5.80 g (59.5 mmol) N,O-dimethylhydroxylamine hydrochloride in 60 ml dichloromethane are added 12.5 g (65.4 mmol) N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride, 4.42 g (32.7 mmol) 1-hydroxybenzothiazol and 16.5 ml (119 mmol) triethylamine. The reaction mixture is stirred for 18 hours at room temperature. It is quenched with saturated sodium hydrogen carbonate solution and the mixture is partitioned between water and dichloromethane. The organic phase is dried over sodium sulfate and evaporated. The residue is chromatographed on a silica gel column with cyclohexane/ethyl acetate as eluent to afford 1-tert-butyl-1H-pyrazole-4-carboxylic acid methoxy-methyl-amide as colorless crystals; HPLC/MS 1.91 min (B), [M+H] 212.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09120805B2
Quelldatensatzuspto-grants-2015_09
ORD IDord-ea6b68daf65d4710bf6eec751004ee32
Quellennotizuspto-grants-2015_09