HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Bromophenoxyacetic acid → 1-(4-(5-Amino-2-(3,4-dimethoxyphenethyl)thiazolo[5,4-d]pyrimidin-7-yl)piperazin-1-yl)-2-(4-bromophenoxy)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Bromophenoxyacetic acid | HCID 74657 | — |
| Reactant | 2-(3,4-Dimethoxyphenethyl)-7-(piperazin-1-yl)thiazolo[5,4-d]pyrimidin-5-amine | HCID 66758068 | — |
| Product | 1-(4-(5-Amino-2-(3,4-dimethoxyphenethyl)thiazolo[5,4-d]pyrimidin-7-yl)piperazin-1-yl)-2-(4-bromophenoxy)ethanone | HCID 66758080 | 74% |
Reaction Steps
This compound was prepared from 2-(3,4-dimethoxyphenethyl)-7-(piperazin-1-yl)thiazolo[5,4-d]pyrimidin-5-amine using 4-bromophenoxyacetic acid in a yield of 74%, according to the procedure for the synthesis of example 50.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09221822B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-09c972d555e74ad0bdea86f658b66fb1 |
| Source note | uspto-grants-2015_12 |