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Chemical Structure| 144657-67-0 Chemical Structure| 144657-67-0

Structure of 144657-67-0

Chemical Structure| 144657-67-0

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Product Details of [ 144657-67-0 ]

CAS No. :144657-67-0
Formula : C13H16N2O3
M.W : 248.28
SMILES Code : CC(C)(C)OC(=O)N1C=C(CO)C2=CC=CN=C12
MDL No. :MFCD11054204

Safety of [ 144657-67-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 144657-67-0 ]

* 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 [ 144657-67-0 ]

[ 144657-67-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 144657-66-9 ]
  • [ 144657-67-0 ]
YieldReaction ConditionsOperation in experiment
85% With sodium tetrahydroborate; In methanol; at 20℃; for 4.0h; A mixture of l-(fer?-butyloxycarbonyl)-3-formyl-7-azaindole (Int-16, 9.8 g, 40 mmol) and sodium borohydride (1.7 g, 44 mmol) in methanol (50 mL) were stirred at rt for 4 h. TLC showed the reaction was complete. Water was added and the mixture was extracted with ethyl acetate. The combined organic phases were washed with water, brine, dried, concentrated, and purified by flash column chromatography to afford alcohol Int-17 (8.4 g, 85%).
47% With sodium tetrahydroborate; ethanol; at 0 - 20℃; for 1.25h;Inert atmosphere; A solution of <strong>[144657-66-9]tert-butyl 3-formyl-1H-pyrrolo[2,3-b]pyridine-1-carboxylate</strong> (420 mg, 1.71 mmol) in ethanol (10 mL) was cooled to 0 C with stirring under nitrogen before sodium borohydride (126.6 mg, 3.35 mmol) was added. The reaction mixture was allowed to warm to rt and stirred for 1.25 h.An aqueous solution of hydrochloric acid (2 M, 4 drops) was added, followed immediately by a saturated solution of sodium bicarbonate (1 mL). The reaction mixture was concentrated in vacuo and the residue partitioned between saturated aqueous sodium bicarbonate solution (50 mL) and ethyl acetate (50 mL). The phases were separated and the aqueous phase further extracted with ethyl acetate (2 x 50 mL). The organic phases were combined, filtered through a cartridgecontaining a hydrophobic frit and the solvent evaporated in vacuo. The residue was dissolved in a1:1 mixture of dichloromethane/methanol (10 mL), concentrated under a stream of nitrogen, anddried in vacuoto give a white solid which was dissolved in dichloromethane (5 mL) and loaded ontoa 25 g SNAP silica cartridge which was purified by flash chromatography, eluting wih a gradient ofSO-100% ethyl acetate in cyclohexane. The required fractions were concentrated in vacuo beforebeing dissolved in a 1:1 mixture of dichloromethane/methanol (10 mL), transferrred to a tarred vial,concentrated under a stream of nitrogen and dried in vacuo to give a white solid; tert-butyl 3- (hydroxymethyl)-1 H-pyrrolo[2,3-b] pyrid me- 1-carboxylate (199.7 mg, 0.80 mmol, 47 % yield).LCMS (2 mm formic) Rt = 0.72 mi m/z= 249 for [MH]
44% With sodium tetrahydroborate; In ethanol; at 20℃; for 4.0h; To a solution of <strong>[144657-66-9]1-(tert-butoxycarbonyl)-3-formyl-7-azaindole</strong> (2.5g, 10.2 mmol) in 16 mL EtOH was added NaBH4 (115mg, 3.05 mmol). The reaction was stirred at ambient temperature for 4h, concentrated and triturated with IN NaOH. The basic solution was extracted with ether and ethylacetate. The organics were washed with water and brine, then dried over Na2S04, filtered and concentrated. The filtrate was concentrated and purified by silica gel chromatography (50% ethylacetate/hexanes) to give tert-butyl 3-(hydroxymethyl)-lH- pyrrolo[2,3-b]pyridine-l-carboxylate (44%). LCMS [M-tert-Bu]+ = 191.1.
To a 10:1 (v/v) MeOH: THF solution (0.2 M) of tert-butyl 3-formyl-l//-pyrrolo[2,3- 6]pyridine-l-carboxylate (1 eq.) from the previous step was added sodium borohydride (2 eq.) at 0 0C. After 3 h of stirring at 0 0C, the mixture was carefully quenched with sat. aq. NH4Cl and then extracted with EtOAc. The combined organic extracts were washed further with brine, dried over Na2SO4, filtered and the filtrate concentrated in vacuo. Purification of the crude product thus obtained via column chromatography (SiO2, CH2Cl2 -> 9:1 (v/v) CH2Cl2: MeOH) afforded the title compound as a pale yellow solid.

 

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