HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966541Generated: October 30, 2026
Benzaldehyde → N*2*-Benzyl-N*1*-(8-methoxy-2-methylquinolin-4-yl)-1-phenylethane-1,2-diamine
https://huagongshe.com/reaction/1966541
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N*1*-(8-Methoxy-2-methylquinolin-4-yl)-1-phenylethane-1,2-diamine | HCID 70276090 | — |
| Product | N*2*-Benzyl-N*1*-(8-methoxy-2-methylquinolin-4-yl)-1-phenylethane-1,2-diamine | HCID 59474813 | 11% |
Reaction Steps
N*1*-(8-Methoxy-2-methylquinolin-4-yl)-1-phenylethane-1,2-diamine (Example 75, 150 mg, 0.488 mmole) and benzaldehyde were stirred at RT for 20 hrs. Molecular sieve (4A) was added and the mixture was heated to 60° C. within 2 hrs. NaBH4 was added and the mixture was stirred for 1 h at RT. The resulting mixture was filtered and extracted with dichloromethane. The organic phases were dried and concentrated. The residue was purified using preparative HPLC (RP-18, water/acetonitrile) to obtain the product (21 mg, 11%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08420670B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-27c07801857346188322936edc9b65d5 |
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| Source note | uspto-grants-2013_04 |
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