HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-((1,1-dimethylethoxy)carbonyl)-beta-alanine → HCID 67040268, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-((1,1-dimethylethoxy)carbonyl)-beta-alanine | HCID 76809 | — |
| Reactant | (S)-2-((tert)-Butoxycarbonyl)amino)butanoic acid | HCID 2755934 | — |
| Reactant | HCID 67040834 | HCID 67040834 | — |
| Product | HCID 67040268 | HCID 67040268 | 23% |
Reaction Steps
The product of Example 13E was reacted with 3-tert-Butoxycarbonylamino-propionic acid using the procedure of Example 70 substituting 3-tert-Butoxycarbonylamino-propionic acid for Boc-Abu-OH to provide the crude title compound which was purified by HPLC with TFA then neutralized with an aqueous sodium carbonate solution to provide the title compound (15 mg, 23%). 1H NMR (300 MHz, DMSO-D6) δ ppm: 1.33 (d, J=6.62 Hz, 6 H) 2.41 (t, J=6.25 Hz, 2 H) 2.83 (t, J=6.25 Hz, 2 H) 3.20 (m, 1 H) 6.97 (d, J=8.46 Hz, 1 H) 7.39 (d, J=8.46 Hz, 2 H) 7.54 (m, 3 H) 7.70 (m, 5 H) 7.95 (s, 1 H) 8.47 (s, 1 H) 8.79 (d, J=8.09 Hz, 1 H) 10.32 (s, 1 H); MS (ESI+) m/z 656/658 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07910595B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-dbe08ede78ee4d93b41ee20732852010 |
| Source note | uspto-grants-2011_03 |