HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986909Generated: October 30, 2026
Indole-2-carboxylic acid → 1h-Indole-2-carboxylic acid {4-[4-(6-fluoro-benzo[b]thiophen-3-yl)-[1,4]diazepan-1-yl]-butyl}-amide
https://huagongshe.com/reaction/1986909
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Indole-2-carboxylic acid | HCID 72899 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Morpholinocarbodiimide | HCID 20187300 | — |
| Reactant | 4-[4-(6-Fluoro-benzo[b]thiophen-3-yl)-[1,4]diazapan-1-yl]butylamine | HCID 57722596 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1h-Indole-2-carboxylic acid {4-[4-(6-fluoro-benzo[b]thiophen-3-yl)-[1,4]diazepan-1-yl]-butyl}-amide | HCID 10205110 | 53.9% |
Reaction Steps
Add indole-2-carboxylic acid (507 mg, 3.15 mmol) to a solution of 4-[4-(6-fluoro-benzo[b]thiophen-3-yl)-[1,4]diazapan-1-yl]butylamine (Example 6) (920 mg, 2.86 mmol), diisopropylethylamine (2.5 mL, 14.3 mmol), 1-hydroxy-1H-benzotriazole (503 mg, 3.72 mmol) and morpholinocarbodiimide (1.39 g, 3.29 mmol) in DMF (10 mL), and stir the solution overnight at room temperature. Remove the solvent under vacuum and dissolve the residue in EtOAc. Wash the organic phase with ether and saturated sodium chloride solution, and dry over MgSO4. Evaporate the solvent under vacuum and purify the crude product by column chromatography (EtOAc/MeOH 7:3) to obtain 716 mg of a colorless solid LC/MS, (LiChrospher 5μ, RP-18, 250 mm CH3CN/Water-gradient 20%→100% (25 min), Flow: 1.5 mL/min) tR=19.89 min, m/z=464.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07550469B2 |
|---|
| Source dataset | uspto-grants-2009_06 |
|---|
| ORD ID | ord-af86d52deb984dd99065ffd4c150c93e |
|---|
| Source note | uspto-grants-2009_06 |
|---|