HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → 3-Iodo-4-methylbenzohydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Methyl 3-iodo-4-methylbenzoate | HCID 13614033 | — |
| Product | 3-Iodo-4-methylbenzohydrazide | HCID 59732500 | — |
Reaction Steps
3-Iodo-4-methyl benzoic acid methyl ester was treated with hydrazine to form 3-Iodo-4-methyl benzoic acid hydrazide. 2-(3-Iodo-4-methyl-phenyl)-[1,3,4]oxadiazole was prepared from 3-iodo-4-methyl benzoic acid hydrazide according to a method analogous to that described in J. of Medicinal Chemistry (2001), 44(8): 1268-85, the entire teachings of which are incorporated herein by reference. Compounds 46, 68, 69, 70, and 71 were prepared via an amide coupling reaction analogous to that described in step A of the synthesis of Compound 1, followed by a Suzuki coupling reaction analogous to that described in step B of the synthesis of Compound 1. The amide coupling reaction and Suzuki coupling reaction are shown for Compound 69 in Scheme XX below:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08202999B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-29707749bb3c4ee5a203b8dcd7886b7e |
| Source note | uspto-grants-2012_06 |