HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → N-[2-(4-(2-Hydroxyethoxy)phenyl)-1-methylethyl]-N-(2-hydroxy-ethyl)-2-hydroxy-2-(2-chloro-thiazol-4-yl)ethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Chloro-4-bromoacetyl-thiazole | HCID 14347762 | — |
| Reactant | HCID 14347764 | HCID 14347764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-[2-(4-(2-Hydroxyethoxy)phenyl)-1-methylethyl]-N-(2-hydroxy-ethyl)-2-hydroxy-2-(2-chloro-thiazol-4-yl)ethanamine | HCID 19380190 | — |
Reaction Steps
Prepared by analogy to Example 30 by reaction of 2-chloro-4-bromoacetyl-thiazole with N-(2-hydroxyethyl)-2-(4-carbomethoxymethoxyphenyl)-1-methylethylamine followed by reduction in methanol with sodium borohydride at room temperature. The crude product is purified on a silica gel column using chloroform/ethyl acetate/methanol=10:9:1 as eluant.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05219852 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-53565f7da74742578dc04cbec6d538ea |
| Source note | uspto-grants-1993_06 |