HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → 2-(3-Quinolylimino)-3,5-diisobutyl-1,3thiazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | 3-Aminoquinoline | HCID 11375 | — |
| Reactant | Isobutylaminehydrochloride | HCID 21133 | — |
| Reactant | (+)-L-Leucine methyl ester | HCID 65105 | — |
| Reactant | L-Leucinol | HCID 111307 | — |
| Reactant | 3-Isothiocyanatoquinoline | HCID 13718421 | — |
| Reactant | (2S)-4-methyl-2-(isobutylamino)pentanol | HCID 22951222 | — |
| Product | 2-(3-Quinolylimino)-3,5-diisobutyl-1,3thiazolidine | HCID 18316332 | — |
Reaction Steps
3-Aminoquinoline was converted to 3-quinoline isothiocyanate according to Method A2c. (1S)-1-(Hydroxymethyl)-3-methylbutylamine was made from (L)-leucine methyl ester as described in Method B1b. The 2-hydroxyethylamine was converted to (2S)-4-methyl-2-(isobutylamino)pentanol as described in Method B4c, Steps 1-2. The alcohol was converted to N-(1S)-1-(chloromethyl)-3-methylbutyl)-N-(isobutyl)ammonium chloride as described in Method B7c. 3-Quinoline isothiocyanate was reacted with N-(1S)-1-(chloromethyl)-3-methylbutyl)-N-(isobutyl)ammonium chloride according to Method C1f to give 2-(3-quinolylimino)-3,5-diisobutyl-1,3thiazolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06353006B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-5ef769350033476a90dd5eeb24076b1d |
| Source note | uspto-grants-2002_03 |