HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373153Generated: October 30, 2026
Hydrochloric Acid → HCID 15027725, compound
https://huagongshe.com/reaction/373153
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 15027724 | HCID 15027724 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15027725 | HCID 15027725 | 94% |
Reaction Steps
5.19 ml of formalin was added to a solution of 2.12 g (free compound: 6.12 mmol) of N-[4-[1-hydroxy-4-[2-(6-methyl-2-pyridyl)ethylamino]butyl]phenyl]methanesulfonamide obtained in Example 3-(4) in 20 ml of methanol. The mixture was refluxed for 30 min. The mixture was cooled at 0° C. and 0.81 g of sodium borohydride was added in small portions thereto. The mixture was stirred at 0° C. for 20 min. 36 ml of 1N hydrochloric acid was added thereto to acidify it. The solution thus obtained was poured into 100 ml of a saturated sodium hydrogencarbonate solution. After extraction with dichloromethane, the organic layer was concentrated to give 2.16 g (yield: 94%) of the intended compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05162347 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-76416c04c93c460d8edf06ba287890a1 |
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| Source note | uspto-grants-1992_11 |
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