HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyloxyacetyl chloride → HCID 54400812, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyloxyacetyl chloride | HCID 177085 | — |
| Reactant | Methyl indolizine-2-carboxylate | HCID 600232 | — |
| Product | HCID 54400812 | HCID 54400812 | — |
Reaction Steps
Following the procedure of Example 3, 2-carbomethoxyindolizine was reacted with benzyloxyacetyl chloride to give 3-benzyloxyacetyl-2-carbomethoxyindolizine (VII) Cyclization of VII with hydrazine and reaction of the resulting pyridazino[4,5-b]indolizin-1-one with POCl3 gave the corresponding chloro compound (VIII). The reaction of VII with 4-(2-pyrimidinyl)-1-piperizinyl)ethyl amine gave the title compound. Treatment with ethereal HCl in ether gave the product as the trihydrochloride salt: m.p. 140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05756501 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-30602f6bc90742fd9f7a2ddf5b7cbc7e |
| Source note | uspto-grants-1998_05 |