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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402253Generated: October 30, 2026

Water → HCID 68650252, compound

https://huagongshe.com/reaction/402253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCyclopropanecarboxaldehydeHCID 123114—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 68649961HCID 68649961—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 68650252HCID 6865025242.3%

Reaction Steps

To a solution of (−)-8-(4-(2-butoxyethoxy)phenyl)-N-(4-(((1-propylimidazol-5-yl)methyl)sulfinyl)phenyl)-1,2,3,4-tetrahydro-1-benzazocine-5-carboxamide (120 mg) in 1,2-dichloroethane (10 ml), cyclopropanecarboxaldehyde (65.6 mg) and sodium triacetoxyborohydride (119 mg) were added. The mixture was stirred at room temperature for overnight. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with saturated NaHCO3, brine, and dried over MgSO4. The volatile materials were removed in vacuo and the residue was purified by column chromatography (basic silicagel, ethyl acetate) to give (−)-8-(4-(2-butoxyethoxy)phenyl)-1-(cyclopropylmethyl)-N-(4-(((1-propylimidazol-5-yl)methyl)sulfinyl)phenyl)-1,2,3,4-tetrahydro-1-benzazocine-5-carboxamide (55 mg)(compound 57) as a yellow amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741943B2
Source datasetuspto-grants-2014_06
ORD IDord-071bf978ac3a4c77b6cbbf63c4923d70
Source noteuspto-grants-2014_06