N-methyl-p-aminophenol
(R)-N2-[(4-amino-3,5-dichlorophenyl)sulphonyl]-N5-[amino(nitroimino)methyl]-ornithine
N-ethyl-N,N-diisopropylamine
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
Conditions | Yield |
---|---|
58% |
(R)-N5-[amino(nitroimino)methyl]-N2-[(2-naphthyl)carbonyl]-ornithine
2-naphthaloyl chloride
A
(R)-N5-[Amino(nitroimino)methyl]-N-[(4-hydroxyphenyl)-methyl]-N2-(2-naphthoyl)-ornithinamide
B
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
Conditions | Yield |
---|---|
A n/a B 36% |
diphenylacetic acid chloride
A
(R,S)-N5-(Aminocarbonyl)-N2-(diphenylacetyl)-N-[(4-hydroxyphenyl)methyl]-ornithinamide
B
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
Conditions | Yield |
---|---|
A n/a B 34% |
N,N,N',N'-tetramethylchlorformamidinium chloride
1-Hydroxy-1,2,3-benzotriazole potassium salt
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
Conditions | Yield |
---|---|
With potassium chloride; potassium tetrafluoroborate |
tetramethylurea
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: oxalyl chloride 2: KBF4,KCl View Scheme |
succinic acid anhydride
B
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
Conditions | Yield |
---|---|
With dmap; benzotriazol-1-ol In ethyl acetate; N,N-dimethyl-formamide |
pyrrolidine
4-bromo-2-methylbenzoic acid
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
N-ethyl-N,N-diisopropylamine
(4-bromo-2-methylphenyl)(pyrrolidin-1-yl)methanone
Conditions | Yield |
---|---|
In tetrahydrofuran; water | 98% |
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
1-t-Butoxycarbonylpiperazine
Conditions | Yield |
---|---|
With triethylamine In water; ethyl acetate; N,N-dimethyl-formamide | 97% |
diisopropylethyl amine
N-ethyl-N-[1-oxo-4-[1-[(phenylmethoxy)carbonyl]-4-piperidinyl]butyl]glycine
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In N-methyl-acetamide; N,N-dimethyl-formamide | 95% |
Oleanolic acid
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
1-benzotriazolyl 3β-hydroxyolean-12-en-28-oate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 12h; | 95% |
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 5h; Inert atmosphere; | 93% |
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 5h; Inert atmosphere; | 93% |
ursolic acid
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 5h; Inert atmosphere; | 93% |
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 5h; Inert atmosphere; | 93% |
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; | |
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran | |
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 4h; |
Betulinic acid
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 5h; Inert atmosphere; | 93% |
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 5h; Inert atmosphere; | 93% |
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; | |
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran |
(2S,4S)-1-(tert-butoxycarbonyl)-4-(8-chloro-2-(4-isopropylthiazol-2-yl)-7-methoxyquinolin-4-yloxy)pyrrolidine-2-carboxylic acid
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide | 92% |
4-methyl-morpholine
1-amino-4-[(tert-butyloxycarbonyl)amino]butane
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
{4-[3-({2-[(4-Cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-phenyl-amino)-propionylamino]-butyl}-carbamic acid tert-butyl ester
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide | 92% |
hedaragenin
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; | 92% |
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine at 20℃; for 12h; | 92% |
oleanolic acid 3-acetate
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine at 20℃; for 12h; | 91% |
(2S,4S)-1-(tert-butoxycarbonyl)-4-(7-methoxy-8-methyl-2-(4-(trifluoromethyl)thiazol-2-yl)quinolin-4-yloxy)pyrrolidine-2-carboxylic acid
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide | 90% |
(2α,3β)-2,3-diacetyloxy-olean-12-en-28-oic acid
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine at 20℃; for 12h; | 90% |
enoxolone
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
1H‐benzo[d][1,2,3]triazol‐1‐yl‐3β‐hydroxy‐11‐oxo‐olean‐12‐en‐30‐oate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 24h; | 90% |
echinocystic acid
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
1-benzotriazolyl 3β,16α-dihydroxyolean-12-en-28-oate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 4h; | 89% |
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; | 86% |
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; Inert atmosphere; | 86% |
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
biotin
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide for 4h; | 89% |
6-[3-(5-fluoro-pyridin-2-yl)-5-methyl-isoxazol-4-ylmethoxy]-pyridazine-3-carboxylic acid
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
2-Amino-2-methyl-1-propanol
N-ethyl-N,N-diisopropylamine
6-[3-(5-fluoro-pyridin-2-yl)-5-methyl-isoxazol-4-ylmethoxy]-pyridazine-3-carboxylic acid (2-hydroxy-1,1-dimethyl-ethyl)-amide
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide | 88% |
2-amino-6-fluoro-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
1H-benzo[d][1,2,3]triazol-1-yl 2-amino-6-fluoropyrazolo[1,5-a]pyrimidine-3-carboxylate
Conditions | Yield |
---|---|
Stage #1: 2-amino-6-fluoro-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid With triethylamine In chloroform for 0.0833333h; Stage #2: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate In chloroform at 60℃; for 1h; | 88% |
Stage #1: 2-amino-6-fluoro-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid With triethylamine In chloroform for 0.0833333h; Stage #2: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate In chloroform at 60℃; for 1h; | 88% |
Stage #1: 2-amino-6-fluoro-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid With triethylamine In chloroform for 0.0833333h; Stage #2: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate In chloroform at 60℃; for 1h; | 88% |
With triethylamine In chloroform at 60℃; for 1h; | 88% |
2-amino-6-chloro-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
1H-benzo[d][1,2,3]triazol-1-yl 2-amino-6-chloropyrazolo[1,5-a]pyrimidine-3-carboxylate
Conditions | Yield |
---|---|
With triethylamine In chloroform at 50℃; for 1h; | 88% |
With triethylamine In chloroform at 50℃; for 1h; | 88% |
With triethylamine In chloroform at 50℃; for 1h; | 88% |
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
2-hydroxy-5-nitroaniline
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 10h; | 86.5% |
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
Conditions | Yield |
---|---|
With triethylamine In chloroform at 50℃; for 0.333333h; | 86% |
In chloroform at 50℃; for 0.333333h; | 86% |
N-methylhex-5-en-1-amine tosylate salt
(1R,2R,4R)-4-(tert-butyldiphenylsilanyloxy)cyclohexane-1,2-dicarboxylic acid 2-tert-butyl ester
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
N-ethyl-N,N-diisopropylamine
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide | 85% |
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
N(1)-(4-chlorophenyl)-2-hydrazino-2-thioxoacetamide
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 10h; | 84.6% |
2-amino-6-(cyanomethyl)-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
1H-benzo[d][1,2,3]triazol-1-yl 2-amino-6-(cyanomethyl)pyrazolo[1,5-a]pyrimidine-3-carboxylate
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 1h; | 84% |
With triethylamine In dichloromethane at 20℃; for 1h; | 84% |
With triethylamine In dichloromethane at 20℃; for 1h; | 84% |
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
4-(piperidin-4-yl)morpholine
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In ethanol; ethyl acetate; N,N-dimethyl-formamide | 84% |
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
5-[4-(1-triphenylmethylimidazol-2-ylamino)butyl]isoxazoline-3-carboxylic acid
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide | 83% |
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
1-cyclobutyl-piperazine
Conditions | Yield |
---|---|
With triethylamine; trifluoroacetic acid In water; dimethyl sulfoxide; acetonitrile | 83% |
IUPAC Name of TBTU (125700-67-6): [benzotriazol-1-yloxy(dimethylamino)methylidene]-dimethylazanium; boron(3+); tetrafluoride
Synonyms:O-Benzotriazol-1-yl-N,N,N',N'-tetramethyluronium tetrafluoroborate; 2-(1H-Benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate
Molecular Formula: C11H16N5O.BF4
Molecular Weight : 321.08 g/mol
EINECS: 423-040-4
storage temp.: 2-8 °C
Melting point: 200 °C
solubility:acetonitrile: 0.1 g/mL, clear
Appearance: white or off-white crystalline powder
Following is the molecular structure of TBTU (125700-67-6):
Safty informations about TBTU (125700-67-6):
Hazard Symbols:Xi,F
Risk Codes :
R36/37/38:Irritating to eyes, respiratory system and skin.
R5 :Heating may cause an explosion.
Safety Description :
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36:Wear suitable protective clothing.
S37/39: Wear suitable gloves and eye/face protection.
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection.
WGK Germany: 3
F: 8-10-21
Hazard Note: Irritant/Flammable
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