HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734418Generated: October 30, 2026
Hydrogen Sulfide → methyl (5-{3-[4-(aminocarbonothioyl)-2-propylphenoxy]-propoxy}-1H-indol-1-yl)acetate
https://huagongshe.com/reaction/734418
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | methyl {5-[3-(4-cyano-2-propylphenoxy)propoxy]-1H-indol-1-yl}acetate | HCID 70971790 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl (5-{3-[4-(aminocarbonothioyl)-2-propylphenoxy]-propoxy}-1H-indol-1-yl)acetate | HCID 57845462 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07592361B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-55255b986b944a3d92e37d5b0e558f0d |
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| Source note | uspto-grants-2009_09 |
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