HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158644Generated: November 1, 2026
Lithium borohydride → HCID 67327277, compound
https://huagongshe.com/reaction/1158644
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 67328162 | HCID 67328162 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67327277 | HCID 67327277 | 16% |
Reaction Steps
To a stirred solution of 1-[(3SR,4RS)-4-(3,4-dichloro-phenyl)-1-(4-methanesulfonyl-piperazine-1-carbonyl)-pyrrolidin-3-yl]-ethanone (XI-1) (2.00 g, 4.46 mmol) in MeOH (40 mL) at −78° C. was added LiBH4 (0.13 g, 4.68 mmol). The temperature was slowly raised to RT (over 1 hour), and the reaction mixture was quenched by addition of H2O. The product was extracted with EtOAc, the combined organic phases were dried over Na2SO4. The two diastereoisomers were separated by column chromatography (SiO2) to yield 0.31 g (16%) of [(3RS,4SR)-3-(3,4-dichloro-phenyl)-4-((RS)-1 hydroxy-ethyl)-pyrrolidin-1-yl]-(4-methanesulfonyl-piperazin-1-yl)-methanone (XII-A-1) as a white solid ES-MS m/e: 450.1 (M+Ht) and 1.02 g (51%) of [(3RS,4SR)-3-(3,4-dichloro-phenyl)-4-((SR)-1-hydroxy-ethyl)-pyrrolidin-1-yl]-(4 methanesulfonyl-piperazin-1-yl)-methanone (XII-1-B-1) as a white solid ES-MS m/e: 450.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812021B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-2326833b59d24a6fbde0aaf9f5e169d6 |
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| Source note | uspto-grants-2010_10 |
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