HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → HCID 178445842, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | (+)-L-Leucine methyl ester | HCID 65105 | — |
| Reactant | L-Leucinol | HCID 111307 | — |
| Reactant | 4-Isothiocyanato-3-(trifluoromethyl)benzonitrile | HCID 18315963 | — |
| Product | HCID 178445842 | HCID 178445842 | — |
Reaction Steps
(1S)-1-(Hydroxymethyl)-3-methylbutylamine was made from (L)-leucine methyl ester as described in Method B1b. The 2-hydroxyethylamine was converted to (1S) -1-(chloromethyl)-3-methylbutanammonium chloride as described in Method B7a. 4-Cyano-2-(trifluoromethyl)phenyl isothiocyanate was reacted with (1S)-1-(chloromethyl)-3-methylbutanammonium chloride according to Method C1c to give (4S)-2-(4-cyano-2-(trifluoromethyl)phenylimino)-4-isobutyl-1,3-thiazolidine. The thiazolidine was reacted with isobutyl bromide according to Method D2f to afford (4S)-2-(4-cyano-2-(trifluoromethyl)phenylimino)-3,4-diisobutyl-1,3-thiazolidine trifluoroacetate salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06353006B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-78e0a9f0ed654e6aab9187da4be70f17 |
| Source note | uspto-grants-2002_03 |