Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 68758033 | HCID 68758033 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58504238 | HCID 58504238 | — |
Reaction Steps
To a mixture of 2-(5-ethoxycarbonyl-1,3,4-thiadiazol-2-yl)-pyridine (8 gm) in ethanol (80 ml), was added sodium borohydride (2.51 gm) in lots at 30° C. It was stirred at 30° C. over a period of 2 h. The solvent was evaporated under vacuum to provide a crude mass. To the crude mass, water (100 ml) was added and it was extracted with dichloromethane (200 ml×2). Combined organic layers was washed with water and concentrated under vacuum to provide title compound in 6.1 gm quantity (92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09175031B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-64aec2ce8964432192a7114f9392bf12 |
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| Source note | uspto-grants-2015_11 |
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