HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(tert-butoxycarbonyl)glycine → HCID 21904412, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(tert-butoxycarbonyl)glycine | HCID 78288 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 12376816 | HCID 12376816 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21904412 | HCID 21904412 | 69% |
Reaction Steps
To a solution of Boc-glycine 130 (1.04 g, 5.88 mmol) and 4-bromobenzylethylamine 131 (1.00 g, 4.90 mmol) in CH2Cl2 (25 mL) at room temperature was added Hunig's base (1.30 mL, 7.35 mmol). The mixture was stirred at room temperature for 16 h. The mixture was poured into water (40 mL) and sat. NaHCO3 (3 mL), then extracted with CH2Cl2 (60 mL), washed with water (100 mL), and dried with Na2SO4. The residue was isolated by column chromatography (50/50/0.1 EtOAc/Hexane/NH4OH), to give 1.30 g of amide 132 as a white crystalline solid in 69% yield. 1H NMR (300 MHz, CDCl3, ppm): δ: 7.37 (d, J=7 Hz, 2H), 7.09 (d, J=7 Hz, 1H), 6.50 (s br, 1H), 5.15 (s br, 1H), 5.01-4.95 (m, 1H), 3.69 (d, J=6 Hz, 2H), 1.39 (d, J=7 Hz, 3H), 1.37 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08324398B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-fa709816834c450b95ce0487cfa321e5 |
| Source note | uspto-grants-2012_12 |