HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685745Generated: November 1, 2026
Sodium borohydride → HCID 67265589, compound
https://huagongshe.com/reaction/1685745
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 86646448 | HCID 86646448 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67265589 | HCID 67265589 | — |
Reaction Steps
To a solution of the 5-formyl-thiophen-2-yl-oxadiazol derivative (1 eq., usual scale 0.02-0.25 mmol) and the appropriate amine (2-40 eq.) in methanol (24 mL/mmol), sodium triacetoxy borohydride (NaBH(OAc)3) (10 eq.) is added. The mixture is stirred for 2 h before NaBH3CN (10 eq.) is added. Stirring of the suspension is continued for 16 h before NaBH4 (20 eq.) is added and stirring is continued for another 16 h at rt. The reaction mixture is diluted with water (4 mL/mmol) and formic acid (4 mL/mmol) and the resulting solution is separated by prep. HPLC (Waters Symmetry C18 19×50 mm, 5 μm, 10 to 95% acetonitrile in water containing 0.5% HCOOH) to give the desired 5-aminomethyl-thiophen-2-yl-oxadiazol derivative as a colourless to pale yellow resin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148410B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-18d412daa6e84e45a80f580647e11457 |
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| Source note | uspto-grants-2012_04 |
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