HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 59854220, compound → HCID 59854175, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 59854220 | HCID 59854220 | — |
| Reactant | HCID 59854253 | HCID 59854253 | — |
| Product | HCID 59854175 | HCID 59854175 | — |
Reaction Steps
For example, methyl 3-amino-2-diphenylmethoxybenzoate A27.12 is reacted with 5-acetyl-4-bromothiazole A27.13 (WO 9317681) to afford after cyclization of the initial displacement product, 5-benzhydryloxy-9-methyl-thiazolo[4,5-b]quinoline-6-carboxylic acid methyl ester A27.14. Reaction with N-bromosuccinimide in hexachloroethane then yields the bromomethyl analog A27.15, and this material is reacted with a trialkyl phosphite in an Arbuzov reaction to give the phosphonate A27.16. The product is then reacted with 3,5-dichlorobenzyl methylamine A27.17 and trimethyl aluminum to afford after deprotection the phosphonate A27.18.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07462721B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-2ffb4644124f47e2ad802d0c0d5f9ef5 |
| Source note | uspto-grants-2008_12 |