HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 136206991, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Hexahydro-1,4-diazepine | HCID 68163 | — |
| Reactant | HCID 136206988 | HCID 136206988 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 136206991 | HCID 136206991 | — |
| Product | HCID 136342878 | HCID 136342878 | — |
Reaction Steps
Displacement of the chloro group of compound 4 with piperazine or [1,4]diazepane using General procedure F provides the compound 47A or 47B. To a stirring solution of 4 (1 eq) in acetonitrile was added piperazine or [1,4]diazepane (large excess) under a blanket of nitrogen. The solution was allowed to stir overnight and then evaporated to dryness. The crude material was purified via silica plug with 9:1 dichloromethane:methanol to afford a white solid, 4-Oxo-2-piperazin-1-ylmethyl-3,4-dihydro-quinazoline-5-carboxylic acid methyl ester, 47A or 2-[1,4]diazepan-1-ylmethyl-4-oxo-3,4-dihydro-quinazoline-5-carboxylic acid methyl ester, 47B.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08236802B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-4ce4b1216b3444119f139f8ec741337b |
| Source note | uspto-grants-2012_08 |