HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(2-Iodo-phenylcarbamoyl)-azetidine-1-carboxylic acid benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | 1-[(Benzyloxy)carbonyl]azetidine-3-carboxylic acid | HCID 10988214 | — |
| Reactant | Iodoaniline | HCID 18447960 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(2-Iodo-phenylcarbamoyl)-azetidine-1-carboxylic acid benzyl ester | HCID 67456254 | — |
Reaction Steps
To 1.0 g (4.57 mmol) iodoaniline in 30 mL acetonitrile were added 2.22 g (5.02 mmol) BOP, 1.78 g (4.57 mmol) azetidine-1,3-dicarboxylic acid monobenzyl ester (route 13, step a), 0.6 mL (4.57 mmol) triethylamine, and the mixture was stirred at room temperature for 16 hours. 0.6 mL (4.57 mmol) triethylamine was added and the mixture was stirred for 2 hours. 2.22 g (5.02 mmol) BOP was added and the mixture was stirred at room temperature for 16 hours. 30 mL 1 M aqueous Na2CO3 was added and the mixture was extracted with EtOAc (2×30 mL), the organic layers were combined, washed with 30 mL brine then dried with Na2SO4. After filtration and evaporation of the solvent the product was purified by column chromatography (silica, heptane/EtOAc 7:3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09346816B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-4d605f15ccd44d6ab539dec074437487 |
| Source note | uspto-grants-2016_05 |