HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393459Generated: October 29, 2026
p-Anisoyl chloride → HCID 57043850, compound
https://huagongshe.com/reaction/393459
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 54376481 | HCID 54376481 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57043850 | HCID 57043850 | 78.1% |
Reaction Steps
To a solution of 4-[[(2,6-dichlorophenyl)carbonyl]amino]-N-[[1-(2-aminoethyl)cyclopentyl]-carbonyl]-L-phenylalanine methyl ester (0.2 mmol, 101 mg) and 4-methoxybenzoyl chloride (0.25 mmol, 52.1 mg) in dichloromethane (1 mL) was added DIPEA (0.3 mmol, 38.7 mg) at room temperature. The reaction mixture was stirred for 15 h at room temperature and then diluted with 20 mL of dichloromethane. The dichloromethane layer was washed successively with water (20 mL) and brine solution (20 mL) and was dried over anhydrous magnesium sulfate. Filtration of the drying agent and concentration of the solvent afforded a crude product which was purified by revesrsed phase HPLC to obtain 0.1 g (78%) of a yellow syrup. HR MS (C33H35Cl2N3O6): Obs. mass, 662.1778. Calcd. mass, 662.1801 (M+Na).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06806365B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-b1bf8bc0712f4e21bb51666e08b5ae83 |
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| Source note | uspto-grants-2004_10 |
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