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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2424962Generated: October 31, 2026

Hydrogen Sulfide → methyl (5-{3-[4-(aminocarbonothioyl)-2-propylphenoxy]-propoxy}-1H-indol-1-yl)acetate

https://huagongshe.com/reaction/2424962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
ReactantDiethylamineHCID 8021—
Reactantmethyl {5-[3-(4-cyano-2-propylphenoxy)propoxy]-1H-indol-1-yl}acetateHCID 70971790—
SolventDimethylformamideHCID 6228—
Productmethyl (5-{3-[4-(aminocarbonothioyl)-2-propylphenoxy]-propoxy}-1H-indol-1-yl)acetateHCID 57845462—

Reaction Conditions

Temperature70 °C

Reaction Steps

Hydrogen sulfide was passed through a solution of methyl{5-[3-(4-cyano-2-propylphenoxy)propoxy]-1H-indol-1-yl}acetate (Example 51, 787 mg, 1.94 mmol) in DMF (15 mL) for 30 minutes at rt. Diethyl amine (0.3 mL, 2.90 mmol) was added, and the solution was heated to 70° C. for 3 h. The reaction mixture was cooled to rt, and the residual H2S was removed by passing argon through the reaction mixture for 30 minutes. The solvent was evaporated under reduced pressure and the residue was filtered through a plug of silica and washed with EtOAc. Concentration of solvent yielded a brown oil which was used in the next step without further purification. LC/MS m/z 441.2 (M+H)+; RT 3.35 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964622B2
Source datasetuspto-grants-2011_06
ORD IDord-baae1535e12540f89a35e269c54f67a5
Source noteuspto-grants-2011_06