Home Cart Sign in  
Chemical Structure| 111222-40-3 Chemical Structure| 111222-40-3

Structure of 111222-40-3

Chemical Structure| 111222-40-3

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 111222-40-3 ]

CAS No. :111222-40-3
Formula : C13H14N2O2
M.W : 230.26
SMILES Code : O=C(C1=C(N)NC(C2=CC=CC=C2)=C1)OCC

Safety of [ 111222-40-3 ]

Application In Synthesis of [ 111222-40-3 ]

* 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 [ 111222-40-3 ]

[ 111222-40-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 57508-48-2 ]
  • [ 70-11-1 ]
  • [ 111222-40-3 ]
YieldReaction ConditionsOperation in experiment
64% The following is representative: <strong>[57508-48-2]ethyl 3-amino-3-iminopropanoate hydrochloride</strong> (3) (8.3 g, 50.0 mmol) and NaOEt (5.1 g, 75.0 mmol) were dissolved in abs. EtOH at 0 C and stirred for 20 min under argon. The mixture was heated to 60 C, and 2-bromo-1-phenylethanone (4b) (5.0 g, 25.0 mmol) was added portion wise over 5 min. After 1.5 h the mixture was cooled to 20 C and the solvent was evaporated under reduced pressure. The residue was diluted with distilled water (20 mL) and extracted with EtOAc (3 × 80 mL). The organic layer was washed with water (3 × 20 mL) and brine (3 × 20 mL). The combined water fractions were back extracted with EtOAc (2 × 20 mL). The organic phases were dried over MgSO4, and the solvent was evaporated under reduced pressure. Purification was by silica-gel column chromatography (EtOAc/n-pentane, 7/3).
64% Pyrrolopyrimidines route 1 The following is representative: Ethyl 2-amino-5-phenyl-lH-pyrrole-3-carboxylate (25) Ethyl 3-amino-3-iminopropanoate hydrochloride (23) (8.3 g, 50.0 mmol) and NaOEt (5.1 g, 75.0 mmol) were dissolved in abs. EtOH at 0 C and stirred for 20 min. under argon. The mixture was heated to 60 C, and 2-bromo-l-phenylethanone (24) (5.0 g, 25.0 mmol) was added portion wise over 5 min. After 1.5 h the mixture was cooled to 20 C and the solvent was evaporated under reduced pressure. The residue was diluted with distilled water (20 mL) and extracted with EtOAc (3 X80 mL). The organic layer was washed with water (3 X20 mL) and brine (3 X20 mL). The combined water fractions were back extracted with EtOAc (2X20 mL). The organic phases were dried over MgSC^, and the solvent was evaporated under reduced pressure. Purification was by silica-gel column chromatography (EtOAc/n-pentane, 7/3). This gave 3.7 g (16.1 mmol, 64%) of a beige solid, mp. 101-104 C; 1H NMR (400 MHz, DMSO-<) delta: 10.72 (s, 1H, NH), 7.50-7.44 (m, 2H), 7.32-25 (m, 2H), 7.1 1-7.05 (m, 1H), 6.46 (d, J=2.4, 1H), 5.65 (s, 2H), 4.15 (q, J=6.8, 2H), 1.25 (t, J=6.8, 3H). 13C NMR (100 MHz, DMSO-<), delta: 165.4, 148.6, 132.6, 129.1 (2C), 125.4, 123.6, 122.8 (2C), 104.0, 93.9, 58.6, 15.2. HRMS (ESI): 231.1 124 (calcd C13H14N2O2, 231.1 128, M+H+). IR (neat, cm"1): 3417, 3328, 1662, 1589, 1281 , 1 120, 757, 691.
  • 2
  • [ 57508-48-2 ]
  • [ 70-11-1 ]
  • [ 2243-35-8 ]
  • [ 55153-12-3 ]
  • [ 111222-40-3 ]
  • [ 582-24-1 ]
 

Historical Records