HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367027Generated: November 1, 2026
Sodium triacetoxyborohydride → HCID 11260625, compound
https://huagongshe.com/reaction/2367027
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 4-Hydroxy-4-(pyridin-2-yl)cyclohexanone | HCID 21187630 | — |
| Reactant | HCID 57803416 | HCID 57803416 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 11260625 | HCID 11260625 | — |
Reaction Steps
N-{2-[(2R,4S)-4-Amino-2-methylpyrrolidin-1-yl]-2-oxoethyl}-3-(trifluoromethyl)benzamide (200 mg, 0.607 mmol) and 4-hydroxy-4-pyridin-2-yl-cyclohexanone (116 mg, 0.607 mmol) were dissolved in 2-propanol (10 mL). After stirring for 30 minutes, sodium triacetoxyborohydride (257 mg, 1.21 mmol) was added and the mixture was stirred at room temperature overnight. TLC indicated complete conversion to desired products in about a 1:1 ratio of two isomers. The reaction mixture was chromatographed on silica gel eluting with dichloromethane to 10% methanol/dichloromethane/0.5% ammonium hydroxide to give 229 mg (75%) as a mixture of isomers. 1H NMR (CDCl3, mixture of isomers) δ 8.53 (m, 1H), 8.13 (bs, 1H), 8.02 (d, 1H), 7.75 (m, 2H), 7.58 (t, 1H), 7.40 (m, 2H), 7.22 (m, 1H), 4.05-4.38 (m, 3H), 3.80 (m, 1H), 3.56 (m, 1H), 3.42 (m, 1H), 3.19 (m, 1H), 3.04 (m, 1H), 2.65 (m, 1H), 2.47 (m, 1H), 2.16 (m, 2H), 1.40-2.00 (m, 7H), 1.43 (d, 3H). LCMS (M+H)+: Higher Rf isomer m/z 505.2; Lower Rf isomer m/z=505.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08697870B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-52b949bb89214198b89dedf38c10c76d |
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| Source note | uspto-grants-2014_04 |
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