Home Cart Sign in  
HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 1111638-01-7 Chemical Structure| 1111638-01-7

Structure of 1111638-01-7

Chemical Structure| 1111638-01-7

*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 [ 1111638-01-7 ]

CAS No. :1111638-01-7
Formula : C14H11BrN2O2S
M.W : 351.22
SMILES Code : O=S(N1C(C)=CC2=CC(Br)=CN=C21)(C3=CC=CC=C3)=O
MDL No. :MFCD15529452

Safety of [ 1111638-01-7 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301
Precautionary Statements:P301+P310
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 1111638-01-7 ]

* 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 [ 1111638-01-7 ]

[ 1111638-01-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1001070-33-2 ]
  • [ 74-88-4 ]
  • [ 1111638-01-7 ]
YieldReaction ConditionsOperation in experiment
64.1% To a solution of diispropylamine (2.52 g, 24.91 mmol) in anhydrous Tetrahydrofuran (THF, 50 mL) n-BuLi (2 M, 9.25 mL, 23.13 mmol) was added dropwise at -78 C and stirring at -78 C under N2 for 30 min. To the mixture a solution of compound 18 (3 g, 8.90 mmol) in anhydrous THF (20 mL) was added and stirred at -78 C for 40 min. To the mixture a solution of compound MeI (3.78 g, 26.69 mmol) in anhydrous THF (20 mL) was added at -78 C and stirred 25 C for 2 h. The mixture was quenched with sat. NH4Cl solution and extracted with Ethyl acetate (EtOAc, 100 mL * 3). The organic phase was washed with brine, dried over Na2SO4, concentrated and purified by column chromatography on silica (PE:EA = 40:1) to give compound 19 as a white solid (2.0 g, 64.1% yield). 1H NMR (400 MHz, DMSO-d6) delta 8.36 (s, 1H, Ar-H), 8.17 (s, 1H, Ar-H), 8.13-8.05 (m, 2H, Ar-H), 7.72-7.70 (t, J = 7.5 Hz, 1H, Ar-H), 7.63-7.59 (t, J = 7.8 Hz, 2H, Ar-H), 6.56 (s, 1H, Ar-H), 2.71 (s, 3H, CH3). ESI-MS m/z: 351.11, 353.11 (M+H)+.
60% Preparation of Method A Intermediate 3: l-Benzenesulfonyl-5-bromo-2-methyl-lH- pyr rolo [2,3-b] pyridine[0426] To a solution of diisopropylamine (2.8 eq, 1.66 mmol, 240 mu) in THF (2 ml) at - 10C is added n-butyllithium (1.6 M in hexane, 2.6 eq, 1.54 mmol, 965 1) dropwise. The mixture is allowed to stir for 30 min and then cooled to -35C. A solution of compound 2 (1 eq., 200 mg, 0.593 mmol) in THF is added dropwise and the mixture is stirred for 30 min at -35C. lodomethane (3 eq, 1.78 mmol, 111 mu) is added in a dropwise fashion and the mixture is stirred for 2 h while warming up to room temperature. The reaction is quenched by addition of a saturated NH4C1 solution, extracted with EtOAc and purified by silica gel chromatography (stepwise gradient of 0 to 15 > EtOAc in hexane). 126 mg (0.359 mmol, 60%>) of compound 3 are obtained. 1H NMR (CDC13, 300 MHz): delta 8.37 (d, J= 2.4 Hz, 1H), 8.12 (m, 2 H), 7.81 (d, J = 2.4 Hz, 1H), 7.58 (m, 1H), 7.50 (m, 2H), 6.24 (d, J= 1.2 Hz, 1H), 2.73 (d, J= 1.2 Hz, 3H). MS (m/z): 352 (M+H).
60% To a solution of diisopropylamine (2.8 eq, 1.66 mmol, 240 muKappa) in THF (2 ml) at -10C is added w-butyllithium (1.6 M in hexane, 2.6 eq, 1.54 mmol, 965 1) dropwise. The mixture is allowed to stir for 30 min and then cooled to -35C. A solution of compound 2 (1 eq., 200 mg, 0.593 mmol) in THF is added dropwise and the mixture is stirred for 30 min at -35C. Iodomethane (3 eq, 1.78 mmol, 1 11 muKappa) is added in a dropwise fashion and the mixture is stirred for 2 h while warming up to room temperature. The reaction is quenched by addition of a saturated NH4C1 solution, extracted with EtOAc and purified by silica gel chromatography (stepwise gradient of 0 to 15% EtOAc in hexane). 126 mg (0.359 mmol, 60%) of compound 3 are obtained. XH NMR (CDC13, 300 MHz): delta 8.37 (d, J= 2.4 Hz, 1H), 8.12 (m, 2 H), 7.81 (d, J= 2.4 Hz, 1H), 7.58 (m, 1H), 7.50 (m, 2H), 6.24 (d, J= 1.2 Hz, lH), 2.73 (d, J= 1.2 Hz, 3H). MS (m/z): 352 (M+H).
57.7% Preparation of 5-bromo-1-(4-bromophenylsulfonyl)-2-methyl-1 H-pyrrolo[2,3-b]pyridine (B-7-5) <n="75"/>B-7-4 B-7-5To a suspension of 5-bromo-1-(phenylsulfonyl)-1 H-pyrrolo[2,3-b]pyridine (B-7-4) (10 g, 0.03 mol) in THF (50 mL) was added dropwise LDA (200 mL, 0.21 M in THF) at -78 0C. The mixture was stirred at -78 C for one hour. Then MeI (5.2 g 0.038 mol) was added dropwise at -78 0C. The reaction was stirred at -7O0C for3 hours, and then stirred at room temperature overnight. LC-MS showed the reaction was complete. Water (200 mL) and EtOAc (100 mLchi3) were added into the mixture. The organic layer was separated, dried over anhydrous Na2SO4 and concentrated to give 5-bromo-1-(4-bromophenylsulfonyl)-2-methyl-1 H- pyrrolo[2,3-b]pyridine (B-7-5) (6 g, 57.7%) as a light yellow solid. 1HNMR (400 MHz, CDCI3): delta 8.390- 8.385 (d, 1 H), 8.176-8.145 (d, 2H), 7.828-7.823 (d, 1 H), 7.613-7.576 (t, 1 H), 7.517-7.479 (t, 2H), 6.254 (s, 1 H), 2.748 (s, 3H).

 

Historical Records

Technical Information

Categories