HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245611Generated: November 2, 2026
Dimethylformamide → 6-amino-5-cyano-1H-indazole-7-carboxylic acid methyl ester
https://huagongshe.com/reaction/245611
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | HCID 57990193 | HCID 57990193 | — |
| Catalyst | Zinc cyanide (Zn(CN)2) | HCID 11186 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 6-amino-5-cyano-1H-indazole-7-carboxylic acid methyl ester | HCID 57990187 | 94% |
Reaction Steps
To a solution of 500 mg (1.85 mmol) of 6-amino-5-bromo-1H-indazole-7-carboxylic acid methyl ester, prepared as in step a in example 16, in 10 mL of N,N-dimethylformamide under an atmosphere of argon is added 135 mg (1.15 mmol) of zinc cyanide and 206 mg (0.185 mmol) of tetrakis(triphenylphsophine)palladium. The reaction mixture is stirred in a microwave oven at 180° C. for 5 minutes. Then, a 1:1 v/v mixture of ethyl acetate and tertbutylmethyl ether and brine are added to the reaction and the phases are separated. The aqueous layer is extracted with tert-butylmethylether. The organic extracts are washed twice with brine, dried over MgSO4 and concentrated in vacuo. The residue is purified by flash chromatography (SiO2, hexane/ethyl acetate 2:1 to 1:1, gradient) to afford 380 mg of product (94%) as a yellowish solid; LC/MS:217/218 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08658801B2 |
|---|
| Source dataset | uspto-grants-2014_02 |
|---|
| ORD ID | ord-8a16bf11ec1f4453a35bc11e4fc6c72a |
|---|
| Source note | uspto-grants-2014_02 |
|---|