HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methyl 3-[(4-chlorobutanoyl)amino]-2-fluoro-5-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Reactant | Methyl 3-amino-2-fluoro-5-nitrobenzoate | HCID 63022631 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-[(4-chlorobutanoyl)amino]-2-fluoro-5-nitrobenzoate | HCID 69358882 | 91% |
Reaction Steps
To a solution of methyl 3-amino-2-fluoro-5-nitrobenzoate (D138) (12 g, 56 mmol, 1 equiv) in CH2Cl2 (150 ml) at room temperature were added NEt3 (11.7 ml, 84 mmol, 1.5 equiv) and 4-chlorobutanoyl chloride (6.9 ml, 61.6 mmol, 1.1 equiv) and the resulting mixture was stirred for 2 h then washed with a 2N aqueous HCl solution and a saturated aqueous NaHCO3 solution, dried over MgSO4 and concentrated in vacuo. Purification of the residue by flash chromatography on silica gel (iso-hexane/AcOEt: 4/1) gave methyl 3-[(4-chlorobutanoyl)amino]-2-fluoro-5-nitrobenzoate (D139) (16.2 g, 91%) as a yellow solid. [M+H]+=319.1, RT=3.12 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07253198B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-da73498e048249afa346cb165be74f26 |
| Source note | uspto-grants-2007_08 |