HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507335Generated: October 26, 2026
2,4-Dimethoxybenzylamine → HCID 16045052, compound
https://huagongshe.com/reaction/507335
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4-Dimethoxybenzylamine | HCID 597250 | — |
| Reactant | (S)-(+)-4-(2,3-Epoxypropoxy)carbazole | HCID 10879208 | — |
| Solvent | Isopropanol ethyl acetate | HCID 22055037 | — |
| Product | HCID 16045052 | HCID 16045052 | 48% |
Reaction Steps
To a solution of (S)-(+)-4-(2,3-Epoxypropoxy)-carbazole (7.56 g, 0.031 mole) in EtOAc/IPA (40/80 mL) was added 2,4-dimethoxybenzylamine (9.48 mL, 0.063 mole) and the reaction mixture was slowly heated to 80-90° C. and then refluxed for 5 hours. Subsequently the reaction mixture was cooled to room temperature and purified following the procedure similar to one described in step 11 for the synthesis of example 23, to afford the desired compound as colorless solid (6 g, 48%) with m.p: 152-154° C. 1H NMR (400 MHz, CDCl3): δ 2.17 (s 1H), 2.88-2.92 (m, 1H), 2.98-3.00 (m, 1H), 3.74-3.87 (m, 8H), 4.18-4.32 (m, 3H), 6.38-6.45 (m, 2H), 6.67 (d, 1H, J=8.0 Hz), 7.05 (d, 1H, J=8.0 Hz), 7.12 (d, 1H, J=8.0 Hz), 7.18-7.40 (m, 4H), 8.08 (s, 1H), 8.21 (d, 1H, J=8.0 Hz). MS m/z: 407.1 (M+1). Chiral purity: 99.96%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786142B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-d800dee02b404e4d907ee9ae4cca8a8a |
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| Source note | uspto-grants-2010_08 |
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