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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016144Generated: November 1, 2026

1,2-Dichloroethane → HCID 57889440, compound

https://huagongshe.com/reaction/1016144

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant893736-84-0HCID 20100120—
ReactantHCID 57889325HCID 57889325—
SolventDichloromethaneHCID 6344—
ProductHCID 57889440HCID 5788944065%

Reaction Steps

(R)-2-Amino-1-((S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)-3-methylbutan-1-one (40 mg, 0.107 mmol), 2′-(methoxycarbonyl)biphenyl-3-carboxylic acid (33 mg, 0.128 mmol), HOBT (20 mg, 0.128 mmol), EDC (25 mg, 0.128 mmol) and triethylamine (0.030 mL, 0.213 mmol) were mixed in methylene chloride (3 mL) at 25° C. with stirring. The reaction was stirred for 20 hours then worked up by adding methylene chloride and washing with sat'd sodium bicarbonate. The methylene chloride layer was dried over sodium sulfate and concentrated in vacuo to give a white glass which was purified over silica gel (3:1 to 1:1 Hexanes/EtOAc) to obtain methyl 3′-((R)-1-((S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)-3-methyl-1-oxobutan-2-ylcarbamoyl)biphenyl-2-carboxylate (40 mg, 0.069 mmol, 65.0% yield) as a white glass. MS found: (M+H)+=577.31.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985861B2
Source datasetuspto-grants-2011_07
ORD IDord-788b329ae2c94eb1be432a4d8377b5f5
Source noteuspto-grants-2011_07