Carbamic acid, N-?(3-?oxocyclopentyl)?-?, 1,?1-?dimethylethyl ester

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CAS:847416-99-3
Purity:98% Min. Package:1G;1KG;100KG
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Products Intro: Product Name:tert-Butyl (3-oxocyclopentyl)carbamate
CAS:847416-99-3
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Carbamic acid, N-?(3-?oxocyclopentyl)?-?, 1,?1-?dimethylethyl ester manufacturers

Carbamic acid, N-?(3-?oxocyclopentyl)?-?, 1,?1-?dimethylethyl ester Basic information
Product Name:Carbamic acid, N-?(3-?oxocyclopentyl)?-?, 1,?1-?dimethylethyl ester
Synonyms:ML213;(3-Oxo-cyclopentyl)-carbamic acid tert-butyl ester;1-(Boc-amino)-3-oxocyclopentane;3-(Boc-aMino)cyclopentanone;Carbamic acid, N-(3-oxocyclopentyl)-, 1,1-dimethylethyl ester;1,1-Dimethylethyl N-(3-oxocyclopentyl)carbamate;2-Methyl-2-propanyl (3-oxocyclopentyl)carbamate
CAS:847416-99-3
MF:C10H17NO3
MW:199.25
EINECS:
Product Categories:CYCLOPENTANE
Mol File:847416-99-3.mol
Carbamic acid, N-?(3-?oxocyclopentyl)?-?, 1,?1-?dimethylethyl ester Structure
Carbamic acid, N-?(3-?oxocyclopentyl)?-?, 1,?1-?dimethylethyl ester Chemical Properties
Boiling point 319.2±31.0 °C(Predicted)
density 1.07±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka11.89±0.20(Predicted)
AppearanceWhite to off-white Solid
InChIInChI=1S/C10H17NO3/c1-10(2,3)14-9(13)11-7-4-5-8(12)6-7/h7H,4-6H2,1-3H3,(H,11,13)
InChIKeyCLOXAWYNXXEWBT-UHFFFAOYSA-N
SMILESC(OC(C)(C)C)(=O)NC1CCC(=O)C1
Safety Information
HS Code 2924297099
MSDS Information
Carbamic acid, N-?(3-?oxocyclopentyl)?-?, 1,?1-?dimethylethyl ester Usage And Synthesis
UsesML-213 is a selective KV7.2 (KCNQ2) and KV7.4 (KCNQ4) channel opener (EC50 values are 230 and 510 nM for KV7.2 and KV7.4 respectively). ML-213 displays >80-fold selectivity against KV7.1, KV7.3 and KV7.5 in a thallium-based fluorescence assay.
Synthesis
2-Cyclopenten-1-one

930-30-3

tert-Butyl carbamate

4248-19-5

Carbamic acid, N-?(3-?oxocyclopentyl)?-?, 1,?1-?dimethylethyl ester

847416-99-3

To a stirred suspension of cyclopent-2-en-1-one (2.50 g, 30.5 mmol) in dichloromethane (60 mL) was added tert-butyl carbamate (3.60 g, 30.5 mmol) and the reaction was stirred for 10-15 minutes. Subsequently, bismuth nitrate (14.70 g, 30.5 mmol) was added in batches and stirring was continued for about 5 hours at room temperature. After completion of the reaction, the reaction mixture was diluted with dichloromethane and filtered through a bed of diatomaceous earth. The filtrate was quenched with saturated sodium bicarbonate solution and the dichloromethane layer was separated. The aqueous layer was extracted with dichloromethane, the organic extracts were combined, dried with anhydrous sodium sulfate and concentrated to give the crude product. The crude product was purified by combiflash chromatography system using hexane solution of 10-15% ethyl acetate as eluent to give tert-butyl (3-oxocyclopentyl)carbamate as white solid (6.50 g, 36% yield). Mass spectrum (MS): 200.20 (M + H).

References[1] Patent: WO2015/25197, 2015, A1. Location in patent: Paragraph 000136
Tag:Carbamic acid, N-?(3-?oxocyclopentyl)?-?, 1,?1-?dimethylethyl ester(847416-99-3) Related Product Information
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