HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671655Generated: October 31, 2026
Sodium borohydride → HCID 178477644, compound
https://huagongshe.com/reaction/1671655
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178477645 | HCID 178477645 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178477644 | HCID 178477644 | — |
Reaction Steps
Sodium borohydride (15 mg) was added to a methanol (1 ml) solution of methyl (6-(4-(ethylsulfonyl)phenoxy)-2-pyridin-2-yl-1H-benzimidazol-5-yl)(hydroxy)acetate (21 mg) obtained in Example 31 (step 2), and the reaction liquid was stirred overnight at 60° C. The solvent was evaporated away under reduced pressure, and the reaction mixture was purified through reversed-phase middle-pressure liquid chromatography (ODS-AS-360-CC (by YMC), mobile phase: water/acetonitrile/0.1% trifluoroacetic acid), and the resulting fraction was diluted with ethyl acetate, washed with aqueous saturated sodium bicarbonate and saturated saline water in that order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure to obtain the entitled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994331B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-6360223bbebe479d943468311ec7796c |
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| Source note | uspto-grants-2011_08 |
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