HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Tert-butyl (r)-4-fluoro-3-[[[n-(benzyloxycarbonyl)-alaninyl]methylamino]methyl]benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Cbz-d-alanine | HCID 70832 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Tert-butyl 4-fluoro-3-(methylaminomethyl)benzoate | HCID 11791275 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl (r)-4-fluoro-3-[[[n-(benzyloxycarbonyl)-alaninyl]methylamino]methyl]benzoate | HCID 131723729 | 73.3% |
Reaction Steps
To a stirred solution of tert-butyl 4-fluoro-3-(methylaminomethyl)benzoate (2.42 g, 10.1 mmole) in DMF (75 mL) was added N-(benzyloxycarbonyl)-D-alanine (2.45 g, 11 mmole) and HOBt.H2O (1.5 g, 11 mmole), followed by DCC (2.4 g, 11.6 mmole). The reaction was stirred for 16 h then was concentrated to dryness. Purification by flash chromatography on silica gel (30% EtOAc/hexanes) gave the title compound (3.29 g, 73%) as a clear oil: 1H NMR (300 MHz, CDCl3) mixture of amide rotamers δ 7.90-7.95 (m, 1H), 7.81 (dd, 1H), 7.31-7.32 (m, 5H), 7.08 (t, 1H), 5.72 & 5.83 (2 d, J=7.8 Hz, 1H), 5.11 (s, 2H), 4.89 (d, J=15.3 Hz, 1H), 4.72-4.77 (m, 1H), 4.47 (d, J=15.3 Hz, 1H), 2.92 & 3.05 (2s, 3H), 1.56 (s, 9H), 1.37 & 1.40(2 d, J=6.8 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06765005B2 |
| Source dataset | uspto-grants-2004_07 |
| ORD ID | ord-82ee9c7dea6840108444f221aded6168 |
| Source note | uspto-grants-2004_07 |