HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylmorpholine → HCID 11602781, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | HCID 6932064 | HCID 6932064 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11602781 | HCID 11602781 | — |
Reaction Steps
7.699 g (25.9 mmol) of N-benzyloxycarbonyl-2(S)-indolinecarboxylic acid prepared as in Example 16 a) are dissolved in tetrahydrofuran (150 ml), under nitrogen. 2.986 g (25.9 mmol) of N-ethylmorpholine are added, at 0° C., followed by 3.54 g (25.9 mmol) of isobutyl chloroformate. After 45 minutes, 1.903 g (25.9 mmol) of n-butylamine are added and the suspension is stirred overnight. Methylene chloride (300 ml) is added and the organic phase is washed with 10% citric acid (3×100 ml) and then NaHCO3 (3×100 ml). After drying and evaporation, a white solid is obtained which is recrystallized from methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06403561B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-48e98f551d8b439ead5a462292f7e276 |
| Source note | uspto-grants-2002_06 |