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Cas:40963-14-2
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inquiryChemical name:2-Amino-2,3-dimethylbutyramide Molecular formula: C6H14N2O Structural formula: Molecular weight: 130.19 CAS No.: 40963-14-2 Physicochemical property: this product is white crystal; m.p.74.5~76℃; soluble in water, ethyl alcohol,
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inquiryProduct Name 2-Amino-2 3-dimethylbutyramide CAS NO. 40963-14-2 Molecular Formula C6H14N2O Molecular Weight 130.19 Appearance white powder
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inquiry2-Amino-2,3-dimethylbutyramide Basic information Product Name: 2-Amino-2,3-dimethylbutyramide Synonyms: 2-AMINO-2,3-DIMETHYL BUTYRAMIDE;2-AMINO-2,3-DIMETHYLBUTACETAMIDE;2-amino-2,3-dimethylbutanamide;2-AMINO-2,3-DIMETHYLBUTACETAMIDE, >93%;2-
Cas:40963-14-2
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inquiryProduct name: 2-Amino-2,3-Dimethylbutyramide CAS No,: 40963-14-2 Molecule Formula:C6H14N2O Molecule Weight:130.19 Purity: 99.0% Package: 25kg/drum Description:White powder Manufacture Standards:Enterprise Standard
Cas:40963-14-2
Min.Order:1 Kilogram
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Cas:40963-14-2
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High quality,stable supply chain.Appearance:white/off-white or light yellow Storage:Store in cool and dry place, keep away from strong light and heat. Package:aluminum bottle,glass bottle,PTFE bottle,cardboard drum Application:This product can be use
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inquiryR & D enterprises have their own stock in stockAppearance:To be subject to the object Package:Customized Application:pharmaceutical intermediates Transportation:Air Port:Shanghai;Guangzhou
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2-amino-2,3-dimethylbutyronitrile
2-amino-2,3-dimethylbutyramide
Conditions | Yield |
---|---|
With water In aq. phosphate buffer at 20℃; pH=7; Concentration; pH-value; Temperature; Solvent; Microbiological reaction; Green chemistry; Enzymatic reaction; | 97.3% |
With ammonium hydroxide; dihydrogen peroxide | |
With sulfuric acid; water |
ammonium hydroxide
2-amino-2,3-dimethylbutyronitrile
2-amino-2,3-dimethylbutyramide
Conditions | Yield |
---|---|
With sulfuric acid In ice-acetone | |
With sulfuric acid In ice-acetone |
2-amino-2,3-dimethylbutyramide
5-(1-ACETYL-3-METHYL-2-IMIDAZOLIDINYL)-2-(4-ISOPROPYL-4-METHYL-5-OXO-2-IMIDAZOLIN-2-YL)NICOTINIC ACID AMMONIUM SALT
Conditions | Yield |
---|---|
With ammonium chloride; potassium tert-butylate In chloroform; toluene | 100% |
2-amino-2,3-dimethylbutyramide
Conditions | Yield |
---|---|
In tetrahydrofuran | 100% |
2-amino-2,3-dimethylbutyramide
2-nitrobenzyl chloride
Conditions | Yield |
---|---|
With triethylamine In chloroform 1.) 1 h, 2.) reflux, 30 min; | 98% |
2-amino-2,3-dimethylbutyramide
2,5-dinitrobenzoyl chloride
Conditions | Yield |
---|---|
With triethylamine In chloroform 1.) 1 h, 2.) reflux, 30 min; | 94% |
2-amino-2,3-dimethylbutyramide
imazapic
Conditions | Yield |
---|---|
With sodium methylate at 120℃; for 1h; Temperature; | 90.8% |
pyridine-2,3-dicarboxylic acid 2-methyl ester
2-amino-2,3-dimethylbutyramide
2-[4,5-dihydro-5-methyl-5-(1-methylethyl)-4-oxo-1H-imidazol-2-yl]nicotinic acid
Conditions | Yield |
---|---|
With sodium methylate at 120℃; for 1h; Temperature; | 90.1% |
Conditions | Yield |
---|---|
With sodium ethanolate at 110℃; for 1h; Temperature; Reagent/catalyst; | 89.2% |
2-amino-2,3-dimethylbutyramide
6-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)furo[2,3-b]pyridine-5-carboxylic acid
Conditions | Yield |
---|---|
In tetrahydrofuran | 88.6% |
2-amino-2,3-dimethylbutyramide
2-[4,5-dihydro-5-methyl-5-(1-methylethyl)-4-oxo-1H-imidazol-2-yl]nicotinic acid
Conditions | Yield |
---|---|
With sodium n-propoxide at 110℃; for 1h; | 88.5% |
2-amino-2,3-dimethylbutyramide
2-[4,5-dihydro-5-methyl-5-(1-methylethyl)-4-oxo-1H-imidazol-2-yl]nicotinic acid
Conditions | Yield |
---|---|
With potassium n-butoxide at 110℃; for 1h; | 88.2% |
2-[(ethyloxy)carbonyl]-3-pyridinecarboxylic acid
2-amino-2,3-dimethylbutyramide
2-[4,5-dihydro-5-methyl-5-(1-methylethyl)-4-oxo-1H-imidazol-2-yl]nicotinic acid
Conditions | Yield |
---|---|
With sodium ethanolate at 110℃; for 1h; Temperature; Reagent/catalyst; | 87.3% |
Conditions | Yield |
---|---|
With potassium n-butoxide at 120℃; for 1h; | 87.3% |
2-amino-2,3-dimethylbutyramide
2-bromobenzene-1,3-dicarboxylic acid dichloride
(+/-)-N,N'-bis(2-carbamoyl-3-methylbut-2-yl)-2-bromobenzene-1,3-dicarboxamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 12h; | 87% |
2-amino-2,3-dimethylbutyramide
A
(S)-α-Methylvaline
B
(+)-(R)-2-amino-2,3-dimethylbutanamide
Conditions | Yield |
---|---|
In water at 37℃; Ochrobactrum anthropi NCIMB 40321; | A 86% B 74% |
With water at 37℃; for 72h; aminopeptidase from Mycobacterium neoaurum ATCC 25795; |
2-amino-2,3-dimethylbutyramide
diethyl 5-ethyl-2,3-pyridinedicarboxylate
imazethapyr
Conditions | Yield |
---|---|
With sodium hydride In toluene at 20℃; for 0.25h; | 85.2% |
2-amino-2,3-dimethylbutyramide
benzaldehyde
(+/-)-2-N-benzylamino-2,3-dimethylbutanamide
Conditions | Yield |
---|---|
With sodium cyanoborohydride; acetic acid In methanol at 20℃; for 48h; | 85% |
3-chlorobenzo[b]thiophen-2-carbonyl chloride
2-amino-2,3-dimethylbutyramide
N-(2-carbamoyl-3-methylbut-2-yl)-3-chlorobenzo[b]thiophene-2-carboxamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 24h; | 85% |
2-amino-2,3-dimethylbutyramide
diethyl quinoline-2,3-dicarboxylate
2-[4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-Yl]-3-quinolinecarboxylic acid
Conditions | Yield |
---|---|
With sodium hydride In toluene at 20℃; for 0.25h; | 83.7% |
pentanal
2-amino-2,3-dimethylbutyramide
Conditions | Yield |
---|---|
In methanol; water | 82% |
2-amino-2,3-dimethylbutyramide
4-chloro-benzoyl chloride
N-(1-Carbamoyl-1,2-dimethyl-propyl)-4-chloro-benzamide
Conditions | Yield |
---|---|
With triethylamine In chloroform 1.) 1 h, 2.) reflux, 30 min; | 81% |
Conditions | Yield |
---|---|
With triethylamine In chloroform 1.) 1 h, 2.) reflux, 30 min; | 81% |
In chloroform Yield given; |
2-amino-2,3-dimethylbutyramide
(+/-)-2-{[2-(aminocarbonyl)-3-methylbut-2-yl]aminocarbonyl}pyridine
Conditions | Yield |
---|---|
Stage #1: 2-Picolinic acid With chloroformic acid ethyl ester; triethylamine In tetrahydrofuran for 0.5h; Stage #2: 2-amino-2,3-dimethylbutyramide In tetrahydrofuran for 3h; | 78% |
2-amino-2,3-dimethylbutyramide
2-bromobenzoic acid chloride
(+/-)-N-(2-carbamoyl-3-methylbut-2-yl)-2-bromobenzenecarboxamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 5h; | 77% |
2-amino-2,3-dimethylbutyramide
diethyl 5-ethyl-2,3-pyridinedicarboxylate
Conditions | Yield |
---|---|
With sodium methylate In toluene for 1h; Heating; | 76.5% |
With hydrogenchloride; potassium tert-butylate In water; toluene |
2-amino-2,3-dimethylbutyramide
o-chlorobenzoyl chloride
Conditions | Yield |
---|---|
With triethylamine In chloroform 1.) 1 h, 2.) reflux, 30 min; | 75% |
2-amino-2,3-dimethylbutyramide
ortho-toluoyl chloride
Conditions | Yield |
---|---|
With triethylamine In chloroform 1.) 1 h, 2.) reflux, 30 min; | 75% |
2-amino-2,3-dimethylbutyramide
4-methyl-benzoyl chloride
(+/-)-N-(1-carbamoyl-1,2-dimethylpropyl)-p-toluamide
Conditions | Yield |
---|---|
With triethylamine In chloroform 1.) 1 h, 2.) reflux, 30 min; | 70% |
With triethylamine In tetrahydrofuran; water | |
With triethylamine In tetrahydrofuran; water | |
With triethylamine In acetone |
Conditions | Yield |
---|---|
With sodium ethanolate; triethylamine In ethanol | 69.9% |
Conditions | Yield |
---|---|
With triethylamine In chloroform 1.) 1 h, 2.) reflux, 30 min; | 68% |
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