HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726382Generated: October 30, 2026
1,1'-Carbonyldiimidazole → HCID 22611465, compound
https://huagongshe.com/reaction/726382
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 1H-Indole-5-Carboxylic Acid | HCID 74280 | — |
| Reactant | 6-amino-3-(dimethyl)amino-1,2,3,4-tetrahydro-9H-carbazole | HCID 22611560 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22611465 | HCID 22611465 | 69% |
Reaction Steps
To a solution of 43.5 mg (0.27 mMol) indole-5-carboxylic acid in 1.5 mL dimethylformamide were added 44.3 mg (0.27 mMol) carbonyldiimidazole resulting in immediate gas evolution. The reaction mixture was stirred for 4 hours at room temperature and then 60.0 mg (0.26 mMol) 6-amino-3-(dimethyl)amino-1,2,3,4-tetrahydro-9H-carbazole were added. After 3 days the reaction mixture was concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with 4:1 dichloromethane:2% ammonium hydroxide in methanol. Fractions shown to contain product were combined and concentrated under reduced pressure to give 66.7 mg (69%) of 6-(indol-5-oyl)amino-3-(dimethyl)amino-1,2,3,4-tetrahydro-9H-carbazole. The compound was converted to its corresponding hydrochloride salt, crystallizing from ethanol:diethyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05708187 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-08bc8f575a554a35bf9681777891266c |
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| Source note | uspto-grants-1998_01 |
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