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CAS No.: | 1072015-52-1 |
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Name: | (R)-Tetrahydrofuran-3-amine hydrochloride |
Molecular Structure: | |
Formula: | C4H9NO.ClH |
Molecular Weight: | 123.582 |
Synonyms: | Josiphos SL-J001-2 |
PSA: | 35.25000 |
LogP: | 1.23630 |
[(3R)-tetrahydrofuran-3-yl]ammonium chloride
Conditions | Yield |
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With sodium tris(acetoxy)borohydride; acetic acid; N-ethyl-N,N-diisopropylamine In 1,2-dichloro-ethane at 20℃; | 91% |
[(3R)-tetrahydrofuran-3-yl]ammonium chloride
Conditions | Yield |
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Stage #1: [(3R)-tetrahydrofuran-3-yl]ammonium chloride; C19H19FN4O2 With N-ethyl-N,N-diisopropylamine In 1,2-dichloro-ethane at 20℃; for 0.166667h; Stage #2: With sodium tris(acetoxy)borohydride; acetic acid In 1,2-dichloro-ethane at 20℃; | 87% |
[(3R)-tetrahydrofuran-3-yl]ammonium chloride
Conditions | Yield |
---|---|
With sodium tris(acetoxy)borohydride; acetic acid; N-ethyl-N,N-diisopropylamine In 1,2-dichloro-ethane at 20℃; | 77% |
Stage #1: [(3R)-tetrahydrofuran-3-yl]ammonium chloride; 1-(6-ethyl-8-fluoro-3-(3-methyl-1,2,4-oxadiazol-5-yl)quinolin-2-yl)piperidin-4-one With N-ethyl-N,N-diisopropylamine In 1,2-dichloro-ethane at 20℃; for 0.166667h; Stage #2: With sodium tris(acetoxy)borohydride; acetic acid In 1,2-dichloro-ethane at 20℃; for 3h; | 68% |
[(3R)-tetrahydrofuran-3-yl]ammonium chloride
Conditions | Yield |
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Stage #1: [(3R)-tetrahydrofuran-3-yl]ammonium chloride; 3-(5-hydroxy-1H-indazo-1-yl)benzoic acid With triethylamine In dichloromethane at 20℃; for 20h; Inert atmosphere; Stage #2: With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide In dichloromethane; ethyl acetate at 0 - 20℃; for 1h; Inert atmosphere; | 73% |
[(3R)-tetrahydrofuran-3-yl]ammonium chloride
Conditions | Yield |
---|---|
With sodium tris(acetoxy)borohydride; acetic acid; N-ethyl-N,N-diisopropylamine In 1,2-dichloro-ethane at 20℃; | 73% |
[(3R)-tetrahydrofuran-3-yl]ammonium chloride
Conditions | Yield |
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With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 120℃; for 12h; | 69% |
[(3R)-tetrahydrofuran-3-yl]ammonium chloride
Conditions | Yield |
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With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 100℃; for 3h; | 67% |
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 100℃; for 3h; | 67% |
[(3R)-tetrahydrofuran-3-yl]ammonium chloride
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 110℃; Inert atmosphere; | 66% |
[(3R)-tetrahydrofuran-3-yl]ammonium chloride
Benzyl bromoacetate
Conditions | Yield |
---|---|
Stage #1: [(3R)-tetrahydrofuran-3-yl]ammonium chloride With triethylamine In tetrahydrofuran at 0℃; for 0.333333h; Stage #2: Benzyl bromoacetate With sodium iodide In tetrahydrofuran at 0 - 20℃; | 60.6% |
4-chloro-5-iodo-6-methyl-pyrimidin-2-ylamine
[(3R)-tetrahydrofuran-3-yl]ammonium chloride
(R)-5-iodo-6-methyl-N4-(tetrahydrofuran-3-yl)pyrimidine-2,4-diamine
Conditions | Yield |
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With triethylamine In ethanol; water Reflux; | 54% |