HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914668Generated: November 1, 2026
Indole-3-Carboxaldehyde → HCID 136347729, compound
https://huagongshe.com/reaction/914668
Participants
| Role | Name | HCID | Charge |
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| Reactant | Indole-3-Carboxaldehyde | HCID 10256 | — |
| Reactant | HCID 58957948 | HCID 58957948 | — |
| Product | HCID 136347729 | HCID 136347729 | 38.3% |
Reaction Steps
Following the procedure described for Example 1 (A), Step A, 2-[1-(3-benzyloxy-phenyl)-5-oxo-4,5-dihydro-2,3,6,10b-tetraaza-benzo[e]azulen-6-yl]-N-isopropyl-N-(6-methoxy-pyridin-3-yl)-acetamide (Preparation 6) (129 mg, 0.219 mmol) was condensed with 1H-indole-3-carbaldehyde (70 mg, 0.48 mmol). Purification by medium pressure chromatography eluting with a solvent gradient (10% EtOAc in hexanes to 100% EtOAc) yielded 60 mg of 2-[1-(3-benzyloxy-phenyl)-4-(1H-indol-3-ylmethylene)-5-oxo-4,5-dihydro-2,3,6,10b-tetraaza-benzo[e]azulen-6-yl]-N-isopropyl-N-(6-methoxy-pyridin-3-yl)-acetamide. 1H NMR (CD3OD) δ 8.13 (m, 1H), 7.64 (m, 2H), 7.23-7.48 (m, 13H), 7.13 (m, 3H), 6.93 (m, 2H), 4.94 (m, 2H), 4.85 (m, 1H), 4.63 (m, 1H), 4.20-4.40 (m, 1H), 3.96 (m, 1H), 3.85 (d, 1H), 0.90-1.05 (m, 6H); MS 716.5 (M+1), 714.6 (M−1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07265104B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-42a34a7bf485433daa82b5017fe69170 |
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| Source note | uspto-grants-2007_09 |
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