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HRID 911849Erstellt: 24. Oktober 2026

1,1'-Carbonyldiimidazole → Tert-butyl 4-(methoxy(methyl)carbamoyl)-3-methylpiperidine-1-carboxylate

https://huagongshe.com/de/reaction/911849

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
EduktMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
EduktN-Boc-3-methyl-4-piperidinecarboxylic acidHCID 4248616—
LösungsmittelDichloromethaneHCID 6344—
ProduktTert-butyl 4-(methoxy(methyl)carbamoyl)-3-methylpiperidine-1-carboxylateHCID 8660164765%

Reaktionsschritte

To a solution of 1-(tert-butoxycarbonyl)-3-methylpiperidine-4-carboxylic acid (3.00 g, 12.3 mmol) in CH2Cl2 (200 mL) was added di(1H-imidazol-1-yl)methanone (2.19 g, 13.6 mmol) portionwise. After the bubbling ceased (−60 minutes), N-methoxymethanamine hydrochloride (1.32 g, 13.6 mmol) was added in one portion. The mixture was allowed to stir overnight at ambient temperature, then was washed with water, 1N HCl, and saturated sodium bicarbonate. The organic layer was dried, filtered, and concentrated to give the desired product (2.29 g, 64.8% yield) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08022223B2
Quelldatensatzuspto-grants-2011_09
ORD IDord-cdda65218f9f41c6be844e9c79cd7bd2
Quellennotizuspto-grants-2011_09