Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 71468391 | HCID 71468391 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70978277 | HCID 70978277 | — |
Reaction Steps
To a solution of 1-(cyclopropylmethyl)-5-{4-[(3-methyl-2,4-dioxoimidazolidin-1-yl)methyl]phenyl}-1H-benzotriazole-4-carbaldehyde (Example 20, 72 mg, 0.18 mmol) in methanol (1.8 mL) was added sodium borohydride (6.8 mg, 0.18 mmol). After 1.5 hours, the mixture was treated with water, diluted with dichloromethane and washed with brine. The organic extract was dried with magnesium sulfate, filtered and concentrated in vacuo. The residue was purified via silica gel chromatography (ethyl acetate/hexane gradient), providing the titled compound: 1H NMR (400 MHz, CDCl3) 7.54 (d, 1H, J=8.8 Hz), 7.42-7.45 (m, 3H), 7.35 (d, 2H, J=8.0 Hz), 5.12 (d, 2H, J=6.4 Hz), 4.65 (s, 2H), 4.55 (d, 2H, J=7.2 Hz), 3.83 (s, 2H), 3.08 (s, 3H), 1.40-1.47 (m, 1H), 0.67-0.71 (m, 2H), 0.51-0.55 (m, 2H) ppm. LRMS m/z (M+H) 406.0 found, 406.2 required.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139576B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-ff8eeba0b24d428c88ed5475cac649dd |
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| Source note | uspto-grants-2015_09 |
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