Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | (2-(Methylthio)ethyl)amine | HCID 87697 | — |
| Reactant | HCID 21344952 | HCID 21344952 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20716559 | HCID 20716559 | — |
Reaction Steps
To a solution of 1-(N-t-butoxycarbonyl-2(S)-aminobutyryl)-indoline-2(S)-carboxylic acid methyl ester (0.5 g, 1.4 mmol) in methanol (2 ml), was added 2-methylthioethylamine (3 ml) under nitrogen, and the resulting solution was stirred at 60° C. for 48 hours. The solution was poured into dichloromethane (20 ml), and washed with 1M potassium hydrogen sulphate, the aqueous layer was extracted with dichloromethane (3×15 ml). The combined organic layers were dried over Na2SO4, and then the solvent was evaporated. A white solid was obtained after column chromatography on silica gel using diethyl ether as eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06335360B1 |
|---|
| Source dataset | uspto-grants-2002_01 |
|---|
| ORD ID | ord-d285dfd85d1249d6bc58a92033a231de |
|---|
| Source note | uspto-grants-2002_01 |
|---|