HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 178491438, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1-[4-(4-Bromobutoxy)3-methoxyphenyl]ethanone | HCID 14407171 | — |
| Reactant | HCID 178419920 | HCID 178419920 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178491438 | HCID 178491438 | 78.6% |
Reaction Steps
A mixture of 3-(4-piperidinyl)-1H indazole (3.2 g, 0.016 mol), 1-[4-(4-bromobutoxy)-3-methoxyphenyl]ethanone (5.0 g, 0.016 mol) K2CO3 (2.2) and acetonitrile (100 ml) was stirred and refluxed for 6hours. The reaction was poured into water and the resulting yellow solid that formed was collected to afford 5.3 g of product. The compound was recrystallized from acetonitrile and then from ethyl acetate to yield 3.0 g (45%) of a slightly yellow solid of 1-[4-[4-[4-(1H-indazol-3-yl)-1-piperidiyl]butoxy]-3-methoxyphenyl]ethanone, m.p.=133°-135° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE039198E1 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-cf3d490e3c1740dcb95fa4f3726cdaa6 |
| Source note | uspto-grants-2006_07 |