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ChemicalBook CAS DataBase List S)-2-((Methoxycarbonyl)aMino)-3-Methylbutanoic acid
1255936-24-3

S)-2-((Methoxycarbonyl)aMino)-3-Methylbutanoic acid synthesis

6synthesis methods
1007882-04-3 Synthesis
(S)-tert-butyl 2-(5-(4-bromophenyl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylate

1007882-04-3
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S)-2-((Methoxycarbonyl)aMino)-3-Methylbutanoic acid

1255936-24-3
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Yield:1255936-24-3 99%

Reaction Conditions:

with trifluoroacetic acid in dichloromethane at 0 - 20; for 5 h;

Steps:

3 Step 3: Synthesis of Compound BB-8

Compound BB-8-3 (3.0 g, 7.65 mmol) was dissolved in dichloromethane (60 mL) and cooled to 0° C., trifluoroacetic acid (20 mL) was dripped gradually, and the reaction was stirred at room temperature for 5 h. The reaction solution was concentrated under reduced pressure to remove the solvent by a rotary evaporator, the resulting oil was neutralized with saturated sodium bicarbonate solution (pH=8) and extracted with ethyl acetate (40 mL×2), the organic phases obtained twice were combined and dried over anhydrous sodium sulfate, the filtrate obtained after filtration was concentrated under reduced pressure to remove the solvent thereby delivering the title compound BB-8 (2.2 g, 99%). LCMS m/z: 292.0 [M+1]+

References:

US2017/253614,2017,A1 Location in patent:Paragraph 0188; 0191

59936-29-7 Synthesis
Boc-L-Proline-methyl ester

59936-29-7
225 suppliers
$6.00/5g

S)-2-((Methoxycarbonyl)aMino)-3-Methylbutanoic acid

1255936-24-3
8 suppliers
inquiry