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Chemical Structure| 881402-27-3 Chemical Structure| 881402-27-3

Structure of 881402-27-3

Chemical Structure| 881402-27-3

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Product Details of [ 881402-27-3 ]

CAS No. :881402-27-3
Formula : C16H19BrN2O3S
M.W : 399.30
SMILES Code : O=C(OC(C)(C)C)N(C1=NC=C(Br)S1)CC2=CC=C(OC)C=C2

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Application In Synthesis of [ 881402-27-3 ]

* 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 [ 881402-27-3 ]

[ 881402-27-3 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 824-94-2 ]
  • [ 405939-39-1 ]
  • [ 881402-27-3 ]
YieldReaction ConditionsOperation in experiment
66% With caesium carbonate; In N,N-dimethyl-formamide; at 80℃; for 1h;Inert atmosphere; 7-Butyl (5-bromothiazol-2-yl)carbamate was dissolved in DMF (40 mL). To the solution were added CS2CO3 (18.0 g, 56.0 mmol) followed by 4-methoxybenzyl chloride (5.1 g, 33.0 mmol). The mixture was stirred at 80 C for 1 h. The reaction mixture was cooled to 25 C, quenched with water (100 mL), and extracted with Et20 (3 x 100 mL). The organic extracts were dried over MgSCL, filtered, and concentrated under reduced pressure. The product, purified by flash column chromatography (hexane: EtOAc; 1 :0 to 7:3), was obtained as a colorless oil (8.7 g, 66 %). (0298) 111 NMR (500 MHz, Chloroform-d) iJtppm); 7.36 (s, 1H), 7.28 - 7.33 (m, 2H), 6.82 - 6.88 (m, 2H), 5.22 (s, 2H), 3.80 (s, 3H), 1.60 (s, 9H); (0299) 13C NMR (126 MHz, Chloroform-d) d (ppm) 161.6, 159.2, 153.3, 138.4, 129.8, 129.4, 113.9, 103.6, 84.1, 55.4, 49.0, 28.4; (0300) HRMS calcd for CieHzoBr^CbS [M+H]+ 399.0373, found 399.0371.
52.4% With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 20℃; To a solution of <strong>[405939-39-1]tert-butyl (5-bromothiazol-2-yl)carbamate</strong> (LXII) (1.3 g, 4.66 mmol) in DCM (23 mL) was added DBU (2.1 mL, 14.04 mmol) was followed by 1-(chloromethyl)-4-methoxybenzene (LXIII) (0.95 mL, 7.01 mmol). The reaction mixture was stirred at room temperature overnight. The solvent was removed under reduced pressure and the residue was purified by silica gel column chromatography (24 g) (0?10% EtOAc/hexanes) to produce tert-butyl (5-bromothiazol-2-yl)(4-methoxybenzyl)carbamate (LXIV) as an off-white solid (974 mg, 2.44 mmol, 52.4% yield). ESIMS found for C16H19BrN2O3S m/z 399.1 (M+H).
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; To a single necked round bottom flask (5-Bromo-thiazol-2-yl)-carbamic acid tert-butyl ester (1.4 g, 5.01 mmol) was dissolved in 25 ml dry DCM. To it 1,8-Diazabicyclo[5.4.0]undec-7-ene(DBU) (2.24 ml, 15.03 mmol) was added followed by 1-Chloromethyl-4-methoxy-benzene (1.02 ml, 7.52 mmol) addition was done and reaction mixture was stirred for overnight. Reaction was quenched by addition of water (20 ml), extracted with DCM (25 ml), Organic layer was separated and washed with brine (30 ml) and dried over anhydrous sodium sulfate, sodium sulfate was filtered and washed with DCM (20 ml) and solvent was evaporated on rotavapour to get required product. The crude material was purified by silica-gel column chromatography, eluding with 4% acetone in hexane. (1.4 g). 1H NMR (400 MHz, CDCl3): delta 1.44(s, 9H), 3.70(s, 3H), 5.11(s, 2H), 6.74 (d, J=8.2 Hz, 2H), 7.21 (d, J=7.9 Hz, 2H), 7.22 (s, 1H). MS (EI) m/z: 400.8 (M+1).
  • 2
  • [ 105-13-5 ]
  • [ 405939-39-1 ]
  • [ 881402-27-3 ]
YieldReaction ConditionsOperation in experiment
2.76 mmol With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 - 20℃; for 2.16667h; Step b. A mixture of <strong>[405939-39-1]tert-butyl (5-bromothiazol-2-yl)carbamate</strong> (3.6 mmol), PP1 (7.9 mmol) and p-methoxybenzyl alcohol (7.2 mmol) in THF (10 ml) was cooled at 0C. DIAD (7.9 mmol) was added dropwise to the reaction mixture at 0C. The reaction mixture was stirred at 0C for 10 min and then at rt for 2 h. The resulting reaction mixture was concentrated under reduced pressure and purified by flash chromatography (0-5% EtOAc in Hexane) yielding tert-butyl (5-bromothiazol-2-yl)(4-methoxybenzyl)carbamate (2.76 mmol). MS: ES- 56 343.1; 1H MR (400 MHz, DMSO-d6) delta ppm 7.57 (s, 1H), 7.22 (d, J=8.4 Hz, 2H), 6.89 (d, J=8.4 Hz, 2H), 5.13 (s, 2H), 3.74 (s, 3H), 1.50 (s, 9H).
1.1 g With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 - 20℃; for 2.16667h; A mixture of <strong>[405939-39-1]tert-butyl (5-bromothiazol-2-yl)carbamate</strong> (l .Og, 3.60 mmol), triphenylphosphine (2.07 g, 7.91 mmol) and p-methoxybenzyl alcohol (0.99 g, 7.19 mmol) in THF (10 ml) was cooled at 0C. DIAD (1.54 ml, 7.91 mmol) was added drop wise to the reaction mixture at 0C. The reaction mixture was stirred at 0C for 10 min and then at rt for 2 h. The resulting reaction mixture was concentrated under reduced pressure and purified by flash chromatography (0-5% EtOAc in Hexane) yielding tert-butyl (5-bromothiazol-2-yl)(4-methoxybenzyl)carbamate (1.1 g, 2.76 mmol). LCMS: Method C, 3.02 min, MS: ES-56 343.1; NMR (400 MHz, DMSO-d6) delta ppm 7.57 (s, 1H), 7.22 (d, J=8.4 Hz, 2H), 6.89 (d, J=8.4 Hz, 2H), 5.13 (s, 2H), 3.74 (s, 3H), 1.50 (s, 9H).
  • 3
  • [ 881402-27-3 ]
  • [ 915411-01-7 ]
  • tert-butyl (5-(1H-indazol-7-yl)thiazol-2-yl)(4-methoxybenzyl)carbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
0.575 g To a stirred solution of lH-indazole-7-boronic acid (0.50 g, 3.09 mmol) and tert-butyl (5- bromothiazol-2-yl)(4-methoxybenzyl)carbamate (0.74 g, 1.85 mmol) in toluene:water (9: 1, 20 ml) was added Na2C03(0.654 g, 6.17 mmol) at rt. The reaction mixture was degassed for 30 min at rt and then treated with Pd(dppf)Cl2(0.22 g, 0.308 mmol). The reaction mixture was heated at 110C for 2 h. The resulting reaction mixture was allowed to cool to rt, poured into water (30 ml) and extracted with EtOAc (2 x 30 ml). The combined organic phase was separated, dried over Na2S04, filtered and concentrated under reduced pressure. The resulting residue was purified by flash chromatography (22% EtOAc in hexane) yielding tert-butyl (5-(lH-indazol-7-yl)thiazol-2-yl)(4- methoxybenzyl)carbamate (0.575 g, 1.32 mmol). LCMS: Method C, 2.67 min, MS: ES+ 437.5; NMR (400 MHz, DMSO-d6) δ ppm: 13.26 (s, 1 H), 8.21 - 8.23 (m, 1 H), 8.03 (s, 1 H), 7.76 (d, J= 8.0 Hz, 1 H), 7.46 (d, J=7.2 Hz, 1 H), 7.29 (d, J=8.4 Hz, 2 H), 7.18 (t, J=7.6 Hz, 1 H), 6.92 (d, J=8.8 Hz, 2 H), 5.24 (s, 2 H), 3.73 (s, 3 H), 1.50 (s, 9 H).
 

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