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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550555Generated: October 31, 2026

Dichloromethane → HCID 15603140, compound

https://huagongshe.com/reaction/550555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57691907HCID 57691907—
Reactant(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexaneHCID 59337591—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 15603140HCID 15603140—

Reaction Steps

To a stirred solution of (1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane (40 mg) and 4-[4-methyl-5-(methylthio)-4H-1,2,4-triazol-3-yl]butanal (40 mg) in 1,2-dichloroethane (4 ml) sodium borohydride (76 mg) and acetic acid (20 μl) were added and the reaction mixture was stirred overnight at room temperature. Then an additional amount of 4-[4-methyl-5-(methylthio)-4H-1, 2,4-triazol-3-yl]butanal (48 mg), sodium borohydride (76 mg) and acetic acid (20 μl) were added and the stirring continued for 2 days then DCM and water were added to the reaction mixture. The solvent was removed under reduced pressure affording a crude product that was purified by chromatography to give the free base of the title compound. To a solution of this compound in DCM (1 mL) HCL 1N in diethylehter was added (0.12 mL) and the solvent removed under reduced pressure to give the title compound (67 mg) as a slightly hygroscopic solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947683B2
Source datasetuspto-grants-2011_05
ORD IDord-cc03ba2d723a4cd384b65cb72bb758ce
Source noteuspto-grants-2011_05