HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyldiazomethane → methyl 2-amino-4-chloro-5-methoxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 2-AMino-4-chloro-5-Methoxy-benzoic acid | HCID 19064965 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | methyl 2-amino-4-chloro-5-methoxybenzoate | HCID 19064933 | 46% |
Reaction Steps
A solution of 2-amino-4chloro-5-methoxybenzoic acid (3.0 g, 15.0 mmol; prepared according to the procedure of Denny, et al., J. Med. Chem. 34:217-222 (1991)) in 70 ml MeOH was treated with excess trimethylsilyl diazomethane. The solution was concentrated and the residue flash chromatographed on silica (9:1 hexane/EtOAc to give the title compound (46%): mp 63°-64° C.; 1H NMR (300 MHz, CDCl3) δ 6 3.83 (s, 3H), 3.90 (s, 3H), 5.48 (bs, 2H), 6.75 (s, 1H), 7.39 (s, 1H); MS (DCI/NH3) m/z 216 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05792767 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-2051251030fc40e2983054b5acb85699 |
| Source note | uspto-grants-1998_08 |