HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 1-[2-(4-Chlorophenyl)ethyl]piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | L-Cysteinylglycine | HCID 439498 | — |
| Reactant | 1-{4-[N-(2-isopropyloxyethyl)-N-chloroacetylamino]benzoyl}-4-[2-(4-chlorophenyl)ethyl]piperazine | HCID 9807391 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[2-(4-Chlorophenyl)ethyl]piperazine | HCID 12235714 | — |
Reaction Steps
Analogously to Example 1, 1.6 g of 1-{4-[N-(2-isopropoxyethyl)-N-chloroacetyl-amino]-benzoyl}-4-[2-(4-chlorophenyl)-ethyl]-piperazine--freed from the corresponding hydrochloride by treatment with a mixture of aqueous ammonia solution/methylene chloride--are reacted with 0.55 g of L-cysteinyl-glycine, yielding 1-{{4-{N-2-isopropoxyethyl)-N-[[[2R]-2-[N'-(carboxymethyl)carbamoyl]-2-amino-ethylmercapto-acetyl]]-amino}-benzoyl}}-4-[2-(4-chlorophenyl)-ethyl]-piperazine. The hemihydrate thereof has a melting point of 85°-87° and an αD25 =-1.5° (c=0.545%, methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05380726 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-7502e364967e4e01878d20fed8cab89f |
| Source note | uspto-grants-1995_01 |