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inquiryA substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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inquiry1-N-Boc-cis-1,4-cyclohexyldiamine Basic information Product Name: 1-N-Boc-cis-1,4-cyclohexyldiamine Synonyms: 1-N-BOC-CIS-1,4-CYCLOHEXYLDIAMINE;CIS-(4-AMINO-CYCLOHEXYL)-CARBAMIC ACID TERT-BUTYL ESTER;Carbamic acid, (cis-4-aminocyclohexyl)-, 1,
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inquiry1-N-Boc-cis-1,4-cyclohexyldiamineAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:pharmaceutical intermediate Transportation:by air, by sea, by express
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tert-butyl ((1S,4S)-4-(1,3-dioxoisoindolin-2-yl)cyclohexyl)carbamate
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
With hydrazine hydrate In ethanol at 80℃; for 2h; | 96% |
di-tert-butyl dicarbonate
cis-1,4-cyclohexanediamine
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
Stage #1: cis-1,4-cyclohexanediamine With hydrogenchloride In methanol at 20℃; for 1h; Stage #2: di-tert-butyl dicarbonate In methanol at 20℃; for 1.16667h; | 66.78% |
(cis-4-azido-cyclohexyl)-carbamic acid tert-butyl ester
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
With hydrogen; 5% palladium-on-charcoal In methanol under 760.051 Torr; for 2h; | 64% |
With hydrogen; 5%-palladium/activated carbon In methanol; toluene at 20℃; under 60804.1 Torr; for 18h; | |
With hydrogen; 5%-palladium/activated carbon In methanol; toluene at 20℃; under 60804.1 Torr; for 18h; |
cis-(4-tert-butoxycarbonylamino-cyclohexyl)-carbamic acid benzyl ester
benzyl alcohol
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
With hydrogen; palladium 10% on activated carbon In ethanol | 58% |
trans-1,4-diaminocyclohexane
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
In methanol at 20℃; for 159.84h; |
(±)-cis-N1-benzyloxycarbonyl-1,4-cyclohexanediamine
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: dichloromethane / 1 h 2: palladium 10% on activated carbon; hydrogen / methanol View Scheme |
cis-(4-tert-butoxycarbonylamino-cyclohexyl)-carbamic acid benzyl ester
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In methanol |
di-tert-butyl dicarbonate
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: dichloromethane / 1 h 2: palladium 10% on activated carbon; hydrogen / methanol View Scheme | |
Multi-step reaction with 3 steps 1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 4 h / 20 °C / Inert atmosphere 2: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0 - 20 °C / Inert atmosphere 3: hydrazine hydrate / ethanol / 2 h / 80 °C View Scheme | |
Multi-step reaction with 3 steps 1: sodium hydroxide / tetrahydrofuran; water / 0 - 20 °C 2: diphenyl phosphoryl azide; triethylamine / toluene / 4 h / 45 - 55 °C 3: hydrogen / palladium 10% on activated carbon / ethanol View Scheme |
trans-tert-butyl 4-hydroxycyclohexylcarbamate
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0 - 20 °C / Inert atmosphere 2: hydrazine hydrate / ethanol / 2 h / 80 °C View Scheme |
trans-4-hydroxycyclohexylamine
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 4 h / 20 °C / Inert atmosphere 2: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0 - 20 °C / Inert atmosphere 3: hydrazine hydrate / ethanol / 2 h / 80 °C View Scheme |
cis-4-tert-butoxycarbonylaminocyclohexane-1-ylcarboxylic acid
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: diphenyl phosphoryl azide; triethylamine / toluene / 4 h / 45 - 55 °C 2: hydrogen / palladium 10% on activated carbon / ethanol View Scheme |
cis-4-aminocyclohexane-1-carboxylic acid
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: sodium hydroxide / tetrahydrofuran; water / 0 - 20 °C 2: diphenyl phosphoryl azide; triethylamine / toluene / 4 h / 45 - 55 °C 3: hydrogen / palladium 10% on activated carbon / ethanol View Scheme |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
6-bromo-2,4-dichloropyrido[2,3-d]pyrimidine
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 3h; | 100% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
Stage #1: tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate; 5-(2-methyl-4-phenoxyphenyl)-4-oxo-4,5-dihydro-3H-1-thia-3,5,8-triazaacenaphthylene-2-carboxylic acid With triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; for 2h; Inert atmosphere; Stage #2: With hydrogenchloride In methanol; water | 100% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
3,5-bis(trifluoromethyl)phenyl carboxylic acid chloride
Conditions | Yield |
---|---|
With triethylamine In benzene at 20℃; for 2h; | 99% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
2-chloro-5-fluoronicotinic acid
tert-butyl N-[(1s,4s)-4-(2-chloro-5-fluoronicotinamido)cyclohexyl]carbamate
Conditions | Yield |
---|---|
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine In tetrahydrofuran; acetonitrile at 0 - 25℃; Inert atmosphere; | 98% |
Stage #1: 2-chloro-5-fluoronicotinic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 0 - 20℃; for 18.15h; Stage #2: tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 18h; |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
2,4,6-trichloropyrido[3,2-d]pyrimidine
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 3h; | 98% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
2-chloronicotinic acid
syn-{4-[(2-chloro-pyridine-3-carbonyl)-amino]-cyclohexyl}-carbamic acid tert-butyl ester
Conditions | Yield |
---|---|
Stage #1: 2-chloronicotinic acid; oxalyl dichloride With N,N-dimethyl-formamide In dichloromethane at 0 - 20℃; for 3.16667h; Stage #2: tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate With N-ethyl-N,N-diisopropylamine In dichloromethane for 18h; | 97% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 0 - 20℃; for 2h; Inert atmosphere; | 96% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
2,4-dichloro-5-bromopyrimidine
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 20℃; | 96% |
With potassium carbonate In acetonitrile at 0 - 20℃; |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
2,4-dichloro-2-methylpyrimidine
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In methanol Heating / reflux; | 95% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
m-anisoyl chloride
cis-[4-(3-methoxy-benzoylamino)-cyclohexyl]-carbamic acid tert-butyl ester
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0℃; for 1h; | 94% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
2-chloro-N,N-dimethylquinazolin-4-amine
tert-butyl (cis-4-{[4-(dimethylamino)quinazolin-2-yl]amino}cyclohexyl)carbamate
Conditions | Yield |
---|---|
In isopropyl alcohol for 576h; Heating; | 93% |
In isopropyl alcohol for 168h; Heating; | 93% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
2-[(3,4-difluorophenyl)amino]-5-fluoronicotinic acid
Conditions | Yield |
---|---|
With 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In dichloromethane for 1h; | 93% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
N-Cbz-L-Phe
C28H37N3O5
Conditions | Yield |
---|---|
With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine In tetrahydrofuran at 20℃; | 91% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
1-[4-chloro-6-(4-morpholinyl)-1,3,5-triazin-2-yl]-2-(difluoromethyl)-4-methoxy-1H-benzimidazole
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; | 90% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In isopropyl alcohol at 170℃; for 1h; | 89% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
3,4-difluorobenzoyl chloride
(cis-4-{[1-(3,4-difluoro-phenyl)-methanoyl]-amino}-cyclohexyl)-carbamic acid tert-butyl ester
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0 - 20℃; for 1h; | 89% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In isopropyl alcohol at 160℃; for 1h; Microwave irradiation; | 89% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
2,4-dichloro-6-bromoquinazoline
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 3h; | 87% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 3h; | 85% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
With tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In toluene at 100℃; for 12h; | 83.2% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
5-fluoro-2-(tetrahydro-2H-thiopyran-4-ylamino)nicotinic acid
tert-butyl [cis-4-({[5-fluoro-2-(tetrahydro-2H-thiopyran-4-ylamino)pyridin-3-yl]carbonyl}amino)cyclohexyl]carbamate
Conditions | Yield |
---|---|
With 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine; HATU In 1-methyl-pyrrolidin-2-one at 20℃; for 0.166667h; pH=8 - 9; | 81% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
4-chloro-2-[(E)-2-(4-chlorophenyl)ethenyl]-6-methylquinazoline
tert-butyl cis-[4-((2-[(E)-2-(4-chlorophenyl)ethenyl]-6-methylquinazolin-4-yl)amino)cyclohexyl]carbamate
Conditions | Yield |
---|---|
With dmap; triethylamine In toluene for 15h; Reflux; | 80.6% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
chloroacetyl chloride
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at -78 - 20℃; | 80% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
2,6-dichloro-5-methylpyrimidine
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In isopropyl alcohol at 150℃; for 0.25h; microwave field; | 79% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
4-chloro-2-methanesulfanylpyrimidine-5-carboxylic acid ethyl ester
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 20℃; | 76% |
With potassium carbonate In acetonitrile at 20℃; | 76% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
4-chloro-2-(methylsulfanyl)pyrimidine-5-carboxaldehyde
Conditions | Yield |
---|---|
In acetonitrile at 20℃; | 73.2% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
2-bromo-5-iodoimidazo[2,1-b][1,3,4]thiadiazole
(cis)-[4-(5-iodo-imidazo[2,1-b][1,3,4]thiadiazol-2-ylamino)-cyclohexyl]-carbamic acid tert-butyl ester
Conditions | Yield |
---|---|
With triethylamine In acetonitrile at 105℃; for 72h; | 71% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
formaldehyd
tert-butyl (1s,4s)-4-(dimethylamino)cyclohexylcarbamate
Conditions | Yield |
---|---|
With sodium cyanoborohydride In methanol at 20℃; | 71% |
tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate
Conditions | Yield |
---|---|
Stage #1: 6-(4-methoxyphenyl)-1-[2-(morpholin-4-yl)ethyl]-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylic acid With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; under 760.051 Torr; for 0.0833333h; Stage #2: tert-butyl N-[(1s,4s)-4-aminocyclohexyl]carbamate With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; under 760.051 Torr; for 14h; | 71% |
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