HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-2-methylpropane → (4S)-2-(4-nitro-1-naphthylimino)-3,4-diisobutyl1,3-thiazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-2-methylpropane | HCID 6555 | — |
| Reactant | HCID 178445847 | HCID 178445847 | — |
| Product | (4S)-2-(4-nitro-1-naphthylimino)-3,4-diisobutyl1,3-thiazolidine | HCID 57275371 | — |
Reaction Steps
(1S)-1-(Hydroxymethyl)-3-methylbutylamine was made from (L)-leucine methyl ester as described in Method B1b. 4-Nitro-1-naphthylamine was converted to 4-nitro-1-naphthyl isothiocyanate according to Method A2b. 4-Nitro-1-naphthyl isothiocyanate was reacted with (1S)-1-(hydroxymethyl)-3-methylbutylamine to Method C2a to give (4S)-2-(4-nitro-1-naphthylimino)-4-isobutyl-1,3-thiazolidine. The thiazolidine was reacted with isobutyl bromide according to Method D2a to give (4S)-2-(4-nitro-1-naphthylimino)-3,4-diisobutyl-1,3-thiazolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06353006B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-a3837cd4472a4746a3f8ae93a624c455 |
| Source note | uspto-grants-2002_03 |