HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 58911823, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Amino(phenyl)acetonitrile--hydrogen chloride (1/1) | HCID 2723717 | — |
| Reactant | Fmoc isothiocyanate | HCID 4154759 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58911823 | HCID 58911823 | 48% |
Reaction Steps
A suspension of α-aminophenylacetonitrile hydrochloride (3.19 g, 18.9 mmol) and Fmoc-isothiocyanate (5.31 g, 18.9 mmol) in DCM was treated with ethyldiisopropylamine (3.62 ml, 20.8 mmol) at 0° C. for 1 hr and then at ambient temperature for 3 hr. The mixture was poured into saturated aqueous sodium bicarbonate and extracted three times into ethyl acetate. The combined organic phases were washed with water and brine, and dried over sodium sulfate and concentrated in vacuo. Flash chromatography on silica gel (ethyl acetate/hexanes) yielded 5-amino-2-(Fmoc-amino)-4-phenylthiazole (3.75 g, 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08110568B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-37143c90f5964c4bb78a2c7b3c36423d |
| Source note | uspto-grants-2012_02 |