HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 15612344, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | tert-Butylacetic acid | HCID 14057 | — |
| Reactant | (+/-)-alpha-amino-alpha-methyl-N-(2-phenylethyl)-1H-indole-3-propanamide | HCID 14560809 | — |
| Reactant | Hydroxybenzothiazole hydrate | HCID 178526942 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 15612344 | HCID 15612344 | 22.6% |
Reaction Steps
A solution of 0.14 g (1.2 mmol) of tert-butylacetic acid in 5 ml of ethyl acetate was treated with 0.367 g (2.4 mmol) of hydroxybenzothiazole hydrate, and 0.247 g (1.2 mmol) of dicyclohexylcarbodiimide. After stirring at room temperature for one hour, the product of Example 12 (0.321 g, 1 mmol) was added, together with a few additional milliliters of ethyl acetate. This mixture was stirred overnight at room temperature, and the crude product isolated. Following purification by column chromatography on silica gel, there was obtained 0.095 g of (±)-α-[(2,3-dimethyl-1-oxobutyl)-amino ]-α-methyl-N-(2-phenylethyl)-1H-indole-3-propanamide, mp 104°-109° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04757151 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-5f11e31640b6411aa61075715cdf0dea |
| Source note | uspto-grants-1988_07 |