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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899900Generated: November 1, 2026

Sodium Carbonate → HCID 178473349, compound

https://huagongshe.com/reaction/1899900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantEthyl 4-amino-1-piperidinecarboxylateHCID 100867—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1,3-dihydro-1-(4-oxocyclohexyl)-2H-benzimidazol-2-oneHCID 21471684—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
SolventChloroformHCID 6212—
ProductHCID 178473349HCID 17847334951.7%

Reaction Steps

A mixture of 1.5 g of 1,3-dihydro-1-(4-oxocyclohexyl)-2H-benzimidazol-2-one, 1.12 g of ethyl 4-amino-1-piperidinecarboxylate, 20 mL of 1,2-dichloroethane, 0.40 mL of glacial acetic acid and 1.79 g of sodium triacetoxyborohydride was stirred at room temperature for 48 h. The reaction mixture was poured into 50 mL chloroform and 50 mL saturated aqueous Na2CO3 and the layers separated. The aqueous layer was extracted with 2×25 mL of chloroform and the combined organic layers dried over MgSO4 and concentrated under reduced pressure. Chromatography of the crude product on silica gel, eluting with 10% methanol in ethyl acetate gave 1.3 g of 1,3-dihydro-1-{trans-4-[1-ethoxycarbonyl-4-piperidinylamino]-1-cyclohexyl}-2H-benzimidazol-2-one as a white solid: 1H NMR (400 MHz, CDCl3) 9.8-9.9 (br m, 1H), 7.30 (m, 1H), 7.11-7.02 (m, 4H), 4.37 (m, 1H), 4.17-4.06 (m, 4H), 3.15 (m, 1H), 2.88 (t, 2H), 2.7 (m, 1H), 2.55 (m, 2H), 1.97 (d, 2H), 1.86 (d, 2H), 1.65 (q, 4H), 1.25 (m, 5H). Analysis calculated for C21H30N4O3C: 65.26, H: 7.82, N: 14.46 found C: 65.20, H: 7.57, N: 14.15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05574044
Source datasetuspto-grants-1996_11
ORD IDord-dd2dd71579b949668334715ef3d985f9
Source noteuspto-grants-1996_11