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Type HazMat fee for 500 gram (Estimated)
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Chemical Structure| 391668-77-2 Chemical Structure| 391668-77-2

Structure of 391668-77-2

Chemical Structure| 391668-77-2

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Product Details of [ 391668-77-2 ]

CAS No. :391668-77-2
Formula : C9H12N2O3S
M.W : 228.27
SMILES Code : CC(C)(C)OC(=O)NC1=NC=C(S1)C=O
MDL No. :MFCD07364348
InChI Key :LKFCHUSAPKBABQ-UHFFFAOYSA-N
Pubchem ID :53393345

Safety of [ 391668-77-2 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 391668-77-2 ]

* 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 [ 391668-77-2 ]

[ 391668-77-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1003-61-8 ]
  • [ 24424-99-5 ]
  • [ 391668-77-2 ]
YieldReaction ConditionsOperation in experiment
With dmap; In tetrahydrofuran; at 20℃; for 12h; [0337] To a solution of 1.0 g of <strong>[1003-61-8]2-aminothiazole-5-carbaldehyde</strong> in 20 ml of THF was added 2.5 g of DIBOC and 1.4 g of DMAP at room temperature, and the mixture was stirred for 12 hours. Water was added to the mixture, and the mixture was extracted with EtOAc. The organic layer was dried over anhydrous MgSO4 and concentrated under reduced pressure, and the resulting crude product was purified by silica gel column chromatography to give 600 mg of t-butyl (5-formylthiazole-2-yl)carbamate (FAB-MS m/z: 229 (M++1)).
In dichloromethane; at 20℃; Compound 75 was prepared from commercially available <strong>[1003-61-8]2-aminothiazole-5-carbaldehyde</strong> by a standard procedure ((BOC)2O, DCM, room temperature).
With dmap; In tetrahydrofuran; at 0 - 20℃; for 1h; Step a. To a solution of <strong>[1003-61-8]2-aminothiazole-5-carbaldehyde</strong> (3.9 mmol) in THF (10 ml) was added DMAP (5.85 mmol) and (BOC)20 (5.85 mmol) at 0C. The reaction mixture was stirred at rt for 1 h. The resulting reaction mixture was poured into water (50 ml) and extracted with EtOAc (3 x 100 ml). The combined organic phase was collected, dried over Na2SC>4, filtered and concentrated under reduced pressure. The resulting residue was purified by flash chromatography (40% EtOAc in hexane) yielding tert-butyl (5-formylthiazol-2-yl) carbamate (2.63 mmol). This material was used directly for the next step without further purification. MS: ES+ 229.05.
 

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• Acyl Group Substitution • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bouveault-Blanc Reduction • Bucherer-Bergs Reaction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Catalytic Hydrogenation • Chan-Lam Coupling Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Chaykovsky Reaction • Corey-Fuchs Reaction • Ester Cleavage • Fischer Indole Synthesis • Grignard Reaction • Hantzsch Dihydropyridine Synthesis • Henry Nitroaldol Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Julia-Kocienski Olefination • Knoevenagel Condensation • Lawesson's Reagent • Leuckart-Wallach Reaction • Mannich Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mukaiyama Aldol Reaction • Nozaki-Hiyama-Kishi Reaction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Amines • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Amines • Reactions with Organometallic Reagents • Reformatsky Reaction • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Carbodiimides and Related Reagents • Specialized Acylation Reagents-Ketenes • Specialized Acylation Reagents-Vilsmeier Reagent • Stetter Reaction • Stobbe Condensation • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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