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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362548Generated: October 26, 2026

3-Chloropropionyl chloride → 2-(3,4-dichlorophenyl)-4-(3,5-dimethylbenzoyl)-1-[3-[5-(phenylmethyl)-(1S,4S)-2,5-diazabicyclo[2.2.1]heptane-2-yl]-1-oxopropyl]piperazine

https://huagongshe.com/reaction/362548

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloropropionyl chlorideHCID 69364—
ReactantDiisopropylethylamineHCID 81531—
Reactant(+)-(3,5-Dimethylbenzoyl)-3-(3,4-dichlorophenyl)piperazineHCID 10292159—
Reactant(1S,4S)-2-Benzyl-2,5-diazabicyclo(2.2.1)heptane--hydrogen bromide (1/2)HCID 14612542—
SolventDichloromethaneHCID 6344—
Product2-(3,4-dichlorophenyl)-4-(3,5-dimethylbenzoyl)-1-[3-[5-(phenylmethyl)-(1S,4S)-2,5-diazabicyclo[2.2.1]heptane-2-yl]-1-oxopropyl]piperazineHCID 2294227029%

Reaction Steps

To a cooled solution of CH2Cl2 (10 mL) containing diisopropylethylamine (0.275 mL, 2.0 mmol) and [3,5-dimethylbenzoyl]-3-(3,4-dichlorophenyl)piperazine (Enantiomer B) (Example 4) (305 mg, 0.84 mmol) was added chloropropionyl chloride (0.075 mL, 0.8 mmol). The reaction mixture was allowed to warm to room temperature. After 20 minutes, (1S,4S)-2-benzyl-2,5-diazabicyclo(2.2.1)heptane 2HBr (297 mg, 0.85 mmol) and diisopropylethylamine (0.275 mL, 2.0 mmol) were added and the mixture was left over night, after which the reaction mixture was concentrated. The product was purified by flash chromatography on flash grade silica gel, eluting with 30:1:0.1 CH2Cl2 /MeOH/NH3 to give a foamy solid (140 mg, 0.23 mmol, 29%), High Res. MS:[M+1]+ calcd. for C34H39Cl2N4O2 605.2450; Found, 605.2465.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869488
Source datasetuspto-grants-1999_02
ORD IDord-3a37d649fd084f85b99ca1d5cc2f3a0f
Source noteuspto-grants-1999_02