HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21055320, compound → HCID 21055321, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21055320 | HCID 21055320 | — |
| Reactant | HCID 21055336 | HCID 21055336 | — |
| Product | HCID 21055321 | HCID 21055321 | — |
Reaction Steps
The title compound (IId-1) is obtained by carrying out the preparation as in example 7 but by replacing, in stage 2, 2-(S)-methyl-3-(2-methoxyphenylthio)propan-1-ol (XXb-1) with 2-(S)-ethyl-3-(2-methoxy-phenylthio)propan-1-ol (XXd-1). This title compound, like the aldehyde (IIb-1), is not isolated but is used in situ in the following reductive amination reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07109234B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-4d2a95291f04459285c1a35ac27b51f7 |
| Source note | uspto-grants-2006_09 |