HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-tert-Butylbenzaldehyde → HCID 86603117, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-tert-Butylbenzaldehyde | HCID 70324 | — |
| Reactant | 1H-Indole-7-carboxylic acid | HCID 74281 | — |
| Reactant | 4-Pyridineethanamine | HCID 83275 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86603117 | HCID 86603117 | 58.3% |
Reaction Steps
81 mg (0.5 mmol) of 4-tert-butyl benzaldehyde and 61 mg (0.5 mmol) of 2-(4-pyridyl)-ethyl amine were dissolved in 2 ml methanol and the solution was stirred for 2 h at rt. 18.5 mg (0.5 mmol) of sodium borohydride were added in portions under nitrogen. The reaction mixture was stirred at rt for 30 min, the solvent was evaporated and the residue was suspended in 4 ml DCM. 88 mg (0.55 mol) of 1H-indole-7-carboxylic acid and 105 mg (0.55 mmol) of EDC.HCl were added and the mixture was stirred at rt over night. The product was purified by column chromatography (silica gel; diethyl ether) to yield 120 mg (58%) product as a colorless oil. MS (ISP) 412.4 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07259183B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-51dd32b747a44534b712392a71598713 |
| Source note | uspto-grants-2007_08 |