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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887937Generated: October 25, 2026

1-Hydroxybenzotriazole hydrate → 1,1-dimethylethyl 2-[4-(aminocarbonyl)-5-propyl-1H-imidazol-2-yl]-2,3-dihydro-1H-indole-1-carboxylate

https://huagongshe.com/reaction/887937

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant1,1-dimethylethyl 2-(4-carboxy-5-propyl-1H-imidazol-2-yl)-2,3-dihydro-1H-indole-1-carboxylateHCID 21914099—
SolventDichloromethaneHCID 6344—
Product1,1-dimethylethyl 2-[4-(aminocarbonyl)-5-propyl-1H-imidazol-2-yl]-2,3-dihydro-1H-indole-1-carboxylateHCID 2191410735.7%

Reaction Steps

1-Hydroxybenzotriazole hydrate (0.00318 mole) was added to a solution of compound 105 (0.00159 mole) in DCM (160 mL) at room temperature. N,N′-methane-tetrayl-biscyclohexanamine (0.00206 mole) was added neat at room temperature. After 60 minutes, NH3 gas was bubbled in for 5 minutes, and a solid precipitated out. The mixture was allowed to sit over the weekend. The mixture was filtered, and the filtrate was extracted with saturated NaHCO3. The organic phases were dried over MgSO4, filtered, and concentrated. The residue was purified by liquid chromatography, yielding 0.21 g of 1,1-dimethylethyl 2-[4-(aminocarbonyl)-5-propyl-1H-imidazol-2-yl]-2,3-dihydro-1H-indole-1-carboxylate (compound 106).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247432B2
Source datasetuspto-grants-2012_08
ORD IDord-6aa8f1cd283c4eb3bd1bad86c6a550ab
Source noteuspto-grants-2012_08