HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride, 3,4,5-trimethoxy- → [1,4-Bis(3,4,5-trimethoxybenzoyl)piperazin-2-yl]methyl diethylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride, 3,4,5-trimethoxy- | HCID 78282 | — |
| Reactant | HCID 70027687 | HCID 70027687 | — |
| Product | [1,4-Bis(3,4,5-trimethoxybenzoyl)piperazin-2-yl]methyl diethylcarbamate | HCID 462383 | 80% |
Reaction Steps
Working again according to a protocol identical to the one used in step 1.3 of Example 1, followed by treating, under the same conditions as those of step 1.4 of Example 1, 0.5 g (1.73 mmol) of 2-(N,N-diethylaminocarbonyloxymethyl)piperazine hydrochloride with 1 g of 3,4,5-trimethoxybenzoyl chloride, 0.83 g of 1,4-bis(3′,4′,5′-trimethoxybenzoyl)-2-(N,N-diethylaminocarbonyloxymethyl)piperazine is obtained. Yield: 80%. Melting point: 128.6° C. Rf=0.35 (3/97 v/v MeOH/CH2Cl2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06531476B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-fe135e91ad7440e69a9d941fbb4373f3 |
| Source note | uspto-grants-2003_03 |