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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364329Generated: November 4, 2026

1,1'-Carbonyldiimidazole → HCID 131728696, compound

https://huagongshe.com/reaction/1364329

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantAzane;hydrateHCID 12896473—
ReactantHCID 66934929HCID 66934929—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131728696HCID 13172869690.3%

Reaction Steps

(Step 3) To (2R)-3-[(tert-butoxycarbonyl)amino]-2-(5-chloro-2-methoxybenzyl)propanoic acid (15 g) in tetrahydrofuran (75 ml) solution, 1,1′-carbonyldiimidazole (7.8 g) was added under ice cooling and the mixture was stirred at room temperature for 1 hour. The reaction solution was cooled to 0° C., 28% ammonia water (15 ml) was added, and the mixture was stirred at room temperature for 30 minutes. To the reaction solution, distilled water, ethyl acetate, and tetrahydrofuran were added, the aqueous layer and the organic layer were separated, and the aqueous layer was extracted with ethyl acetate. The combined organic layer was successively washed with saturated potassium hydrogensulfate aqueous solution and saturated saline, dried over with anhydrous sodium sulfate, and concentrated until a small amount of ethyl acetate remained. Hexane was added to the concentrated solution, and the precipitated solid was collected by filtration to obtain the title compound (13.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888348B2
Source datasetuspto-grants-2011_02
ORD IDord-73b0cd03553a4c48aacaba51d1c04b10
Source noteuspto-grants-2011_02