HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658222Generated: October 29, 2026
Water → N-[(3R)-1-azabicyclo[2.2.2]octan-3-yl]-7-[(Z)-N'-hydroxycarbamimidoyl]-1-benzothiophene-2-carboxamide;dihydrochloride
https://huagongshe.com/reaction/658222
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 68431784 | HCID 68431784 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[(3R)-1-azabicyclo[2.2.2]octan-3-yl]-7-[(Z)-N'-hydroxycarbamimidoyl]-1-benzothiophene-2-carboxamide;dihydrochloride | HCID 87452962 | — |
Reaction Steps
120 mg (0.43 mmol) of N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-cyano-1-benzothiophene-2-carboxamide hydrochloride, 45.0 mg (0.65 mmol) of hydroxylamine hydrochloride and 119.2 mg (0.86 mmol) of potassium carbonate in 1.5 ml of an 8:1 mixture of water and ethanol are heated at 80° C. for 18 h. The mixture is purified by preparative HPLC. The product fractions are combined and concentrated, acetonitrile and 1N aqueous hydrochloric acid (3:1) are added and the mixture is then again concentrated and dried under high vacuum. 58 mg (30.3% of theory) of the title compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076355B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-9a0c6d9d0f754f1187b69885322671c3 |
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| Source note | uspto-grants-2011_12 |
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