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Chemistry
Organic Building Blocks
Thiazoles
tetrahydrobenzo
Ethyl 2-bromo-4,5,6,7-tetrahydrobenzo[d]thiazole-6-carboxylate
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tetrahydrobenzo
4,5,6,7-tetrahydrobenzo[d]thiazole

[ CAS No. 1547445-11-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
3d Animation Molecule Structure of 1547445-11-3
Chemical Structure| 1547445-11-3
Chemical Structure| 1547445-11-3
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Quality Control of [ 1547445-11-3 ]

COA NMR CNMR HPLC LC-MS

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Product Details of [ 1547445-11-3 ]

CAS No. :1547445-11-3 MDL No. :MFCD27918600
Formula : C10H12BrNO2S Boiling Point : -
Linear Structure Formula :- InChI Key :SIKMIRQRUUUIKQ-UHFFFAOYSA-N
M.W : 290.18 Pubchem ID :84008242
Synonyms :

Safety of [ 1547445-11-3 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313 UN#:N/A
Hazard Statements:H315-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1547445-11-3 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1547445-11-3 ]

[ 1547445-11-3 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 110-91-8 ]
  • [ 1547445-11-3 ]
  • [ 1845723-06-9 ]
YieldReaction ConditionsOperation in experiment
at 115℃; for 6h; 2 General procedure for the synthesis of U6 General procedure for the synthesis of U6 A mixture of U5 (0.26 g, 0.73 mmol) and morpholine (1.5 mL) was heated to 130 °C with stirring for 3h. The reaction mixture was diluted with water (20 mL) and extracted with EtOAc (20 mL x 2). The organic layer was dried over MgS04 and concentrated in vacuo. The resulting crude residue was purified by flash column cliromatography (rc-hexane: EtOAc = 10: 1) to give U6. 1H NMR (400MHz, DMSO-d6) δ 7.45 - 7.47 (m, 2H), 7.30 - 7.39 (m, 3H), 5.37 (s, 2H), 4.18 (q, J= 6.8 Hz, 2H), 3.69 - 3.71 (m, 4H), 3.48 - 3.53 (m, 4H), 1.21 (t, J= 6.8 Hz, 3H).
Reference： [1]Current Patent Assignee: INSTITUT PASTEUR - WO2015/193506, 2015, A1 Location in patent: Page/Page column 59
  • 2
  • [ 134136-00-8 ]
  • C10H12BrNO2S [ No CAS ]
YieldReaction ConditionsOperation in experiment
With tert.-butylnitrite; copper(ll) bromide In acetonitrile for 3h; Reflux; 2 General procedure for the synthesis of Z3-a and Z3-b General procedure for the synthesis of Z3-a and Z3-b To a stirred solution of Z2-a or Z2-b (5.87 mmol) in acetonitrile (20 mL) were added copper(II)bromide (7.04 mmol) and fert-butyl nitrate (14.67 mmol). The reaction mixture was stirred at reflux temperature for 3 hours. The reaction mixture was diluted with methylene chloride (20 mL) and washed with brine (20 mL). The organic layer was dried over anhydrous MgS0 and concentrated in vacuo. The crude product was purified by flash column chromatography to give Z3-a or Z3-b. Z3-a; ]H NM (400 MHz, CDC13) δ 4.16 - 4.21(m , 2H), 2.72 - 3.01 (m, 5H), 2.21 - 2.27 (m, 1H), 1.95 - 2.01 (m, 1H), 1.22 - 1.28 (m, 3H). Z3-b; 1H NMR (400 MHz, CDC13) δ 4.17 - 4.21 (m , 2H), 3.77 - 4.01 (m, 4H), 3.39 - 3.42 (m, 4H), 2.85 - 2.89 (m, 2H), 2.59 - 2.79 (m, 3H), 2.18 - 2.24 (m, 1H), 1.90 - 1.98 (m, 1H), 1.25 - 1.30 (m, 3H).
Reference： [1]Current Patent Assignee: INSTITUT PASTEUR - WO2015/193506, 2015, A1 Location in patent: Page/Page column 64-65
  • 3
  • [ 39086-05-0 ]
  • [ 1547445-11-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: ethanol / 2 h / Reflux 2: tert.-butylnitrite; copper(ll) bromide / acetonitrile / 3 h / Reflux
Reference： [1]Current Patent Assignee: INSTITUT PASTEUR - WO2015/193506, 2015, A1
  • 4
  • [ 17159-79-4 ]
  • [ 1547445-11-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: toluene-4-sulfonic acid; N-Bromosuccinimide / toluene / 2 h / 115 °C 2: ethanol / 2 h / Reflux 3: tert.-butylnitrite; copper(ll) bromide / acetonitrile / 3 h / Reflux
Reference： [1]Current Patent Assignee: INSTITUT PASTEUR - WO2015/193506, 2015, A1

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Technical Information

• Acid-Catalyzed α -Halogenation of Ketones • Acyl Group Substitution • Addition of a Hydrogen Halide to an Internal Alkyne • Alcohols Convert Acyl Chlorides into Esters • Alcohols from Haloalkanes by Acetate Substitution-Hydrolysis • Alcohols React with PX3 • Alcoholysis of Anhydrides • Alkyl Halide Occurrence • Alkylation of an Alkynyl Anion • Amines Convert Esters into Amides • An Alkane are Prepared from an Haloalkane • Benzylic Oxidation • Birch Reduction • Birch Reduction of Benzene • Blanc Chloromethylation • Bouveault-Blanc Reduction • Catalytic Hydrogenation • Claisen Condensations Produce β-Dicarbonyl Compounds • Claisen Condensations Produce β-Dicarbonyl Compounds • Complete Benzylic Oxidations of Alkyl Chains • Complete Benzylic Oxidations of Alkyl Chains • Complex Metal Hydride Reductions • Conversion of Amino with Nitro • Convert Esters into Aldehydes Using a Milder Reducing Agent • Convert Haloalkanes into Alcohols by SN2 • Decarboxylation of 3-Ketoacids Yields Ketones • Deprotection of Cbz-Amino Acids • Deprotonation of Methylbenzene • Directing Electron-Donating Effects of Alkyl • Electrophilic Chloromethylation of Polystyrene • Ester Cleavage • Ester Hydrolysis • Friedel-Crafts Alkylation of Benzene with Acyl Chlorides • Friedel-Crafts Alkylation of Benzene with Carboxylic Anhydrides • Friedel-Crafts Alkylation of Benzene with Haloalkanes • Friedel-Crafts Alkylation Using Alkenes • Friedel-Crafts Alkylations of Benzene Using Alkenes • Friedel-Crafts Alkylations Using Alcohols • Friedel-Crafts Reaction • General Reactivity • Grignard Reaction • Grignard Reagents Transform Esters into Alcohols • Groups that Withdraw Electrons Inductively Are Deactivating and Meta Directing • Halogenation of Alkenes • Halogenation of Benzene • Hantzsch Pyridine Synthesis • Hiyama Cross-Coupling Reaction • Hydrogenation to Cyclohexane • Hydrogenolysis of Benzyl Ether • Ketones Undergo Mixed Claisen Reactions to Form β-Dicarbonyl Compounds • Kinetics of Alkyl Halides • Kumada Cross-Coupling Reaction • Methylation of Ammonia • Methylation of Ammonia • Nitration of Benzene • Nucleophilic Aromatic Substitution • Nucleophilic Aromatic Substitution with Amine • Oxidation of Alkyl-substituted Benzenes Gives Aromatic Ketones • Preparation of Alkylbenzene • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reactions of Dihalides • Reactions with Organometallic Reagents • Reduction of an Ester to an Alcohol • Reduction of an Ester to an Aldehyde • Reductive Removal of a Diazonium Group • Reverse Sulfonation——Hydrolysis • Specialized Acylation Reagents-Carbodiimides and Related Reagents • Stille Coupling • Substitution and Elimination Reactions of Alkyl Halides • Sulfonation of Benzene • Suzuki Coupling • The Acylium Ion Attack Benzene to Form Phenyl Ketones • The Claisen Rearrangement • The Cycloaddition of Dienes to Alkenes Gives Cyclohexenes • The Nitro Group Conver to the Amino Function • Transesterification • Vilsmeier-Haack Reaction • Williamson Ether Syntheses
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