HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252501Generated: October 29, 2026
Hydrazine hydrate (1:1) → HCID 11680306, compound
https://huagongshe.com/reaction/252501
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | HCID 59425473 | HCID 59425473 | — |
| Reactant | HCID 59425954 | HCID 59425954 | — |
| Solvent | Pyrrolidine | HCID 31268 | — |
| Product | HCID 11680306 | HCID 11680306 | 54% |
Reaction Steps
1-(1-Ethyl-6-methoxy-1H-indol-3-yl)-ethanone (100 mg, 0.46 mmol), prepared from 1-ethyl-6-methoxy-1H-indole by the procedure described in example 1L, is heated with 1.5 mL of dimethylformamide dimethyl acetal and 100 μL pyrrolidine at 110° C. overnight. The DMF dimethyl acetal is removed in vacuo. The residue is redissolved in 3 mL of acetic acid, hydrazine hydrate (70 μL, 1.38 mmol) is added, and the mixture is heated to 100° C. for 2 h. The acetic acid is removed in vacuo, and the residue is partitioned between EtOAc and saturated NaHCO3. The organic phase is dried and concentrated and the product purified by silica gel chromatography (EtOAc/Hex, 1/1) to give 59 mg of 1-ethyl-6-methoxy-3-(2H-pyrazol-3-yl)-1H-indole (54%) as a colorless semisolid. Trituration in Et2O gives a white crystalline powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07868037B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-b44aac757e7b4fc2ac123ac3dad526ab |
|---|
| Source note | uspto-grants-2011_01 |
|---|