HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165589Generated: October 28, 2026
HCID 178458742, compound → HCID 178458741, compound
https://huagongshe.com/reaction/1165589
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178458742 | HCID 178458742 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178458741 | HCID 178458741 | 43.8% |
Reaction Steps
A warm slurry of 3-(1-methylethoxy)-5-(phenylmethoxy )-N-1H-tetrazol-5-yl-benzo[b]thiophene-2carboxamide (1.9 g, 5 mmoles) and 20% palladium on carbon (0.5 g) in acetic acid (250 mls) is shaken under hydrogen (50 psig) in a Parr apparatus. After three hours additional catalyst (0.5 g) is added and the mixture shaken at ambient temperature for 15 hours. The catalyst is removed by filtration and rinsed with warm acetic acid (200 mls). The filtrate is stripped of solvent under reduced pressure and two portions (50 mls) of toluene are added to, then stripped from the residue, leaving the crystalline product. Recrystallization from methanol gave the pure 3-(1-methylethoxy)-5-hydroxy -N-lH-tetrazol-5-yl-benzo[b]thiophene-2-carboxamide (0.7 g): mp=258° C. (dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04910317 |
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| Source dataset | uspto-grants-1990_03 |
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| ORD ID | ord-fd43968efee84644a8f08f3a5e8bd7f2 |
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| Source note | uspto-grants-1990_03 |
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