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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloropropionyl chloride | HCID 69364 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (+)-(3,5-Dimethylbenzoyl)-3-(3,4-dichlorophenyl)piperazine | HCID 10292159 | — |
| Reactant | (1S,4S)-2-Benzyl-2,5-diazabicyclo(2.2.1)heptane--hydrogen bromide (1/2) | HCID 14612542 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 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 | HCID 22942270 | 29% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05869488 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-3a37d649fd084f85b99ca1d5cc2f3a0f |
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| Source note | uspto-grants-1999_02 |
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