HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006268Generated: November 2, 2026
Cyclopropanecarboxaldehyde → HCID 22676744, compound
https://huagongshe.com/reaction/1006268
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropanecarboxaldehyde | HCID 123114 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22676732 | HCID 22676732 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22676744 | HCID 22676744 | 78.3% |
Reaction Steps
Cyclopropanecarboxaldehyde (168 mg, 2.4 mmol) was added to a stirred mixture of ethyl 5-amino-3-(4-tert-butylphenyl)-1-(3-methoxybenzyl)-1H-indole-2-carboxylate (Example 160, 530 mg, 1.2 mmol) in toluene (12 mL) and molecular sieves (2 g). The reaction was stirred for 16 h and then filtered using toluene to rinse. The filtrate was concentrated in vacuo and the residue was dissolved in methanol (12 mL). Sodium borohydride (15 mg, 1.2 mmol) was added and the reaction was stirred for 2 h. The mixture was diluted with ethyl acetate (50 mL), washed with water and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo. Flash chromatography of the residue over silica gel using 4:1 hexane/ethyl acetate afforded 480 mg (78%) of desired product. The product had: 1H NMR (300 MHz, acetone-D6) δ 7.45-7.48 (m, 2 H), 7.34-7.38 (m, 2 H), 7.31 (d, 1 H), 7.18 (dd, 1 H), 6.87 (dd, 1H), 6.77 (ddd, 1 H), 6.65-6.70 (m, 2 H), 6.62 (d, 1 H), 5.75 (s, 2 H), 4.68 (s, 1 H), 4.08 (q, 2 H), 3.69 (s, 3 H), 2.89 (d, 2 H), 1.37 (s, 9 H), 1.00-1.10 (m, 1 H), 0.93 (t, 3 H), 0.42-0.49 (m, 2 H), 0.16-0.25 (m, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06787651B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-3cc6863955fe480280af80d962ce51ec |
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| Source note | uspto-grants-2004_09 |
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