ChemicalBook >> CAS DataBase List >>6-Bromo-N-methyl-2-naphthalenecarboxamide

6-Bromo-N-methyl-2-naphthalenecarboxamide

CAS No.
426219-35-4
Chemical Name:
6-Bromo-N-methyl-2-naphthalenecarboxamide
Synonyms
6-BROMO-N-METHYL-2-NAPHTOAMIDE;6-bromo-N-methyl-2-naphthamide;6-Bromo-N-methyl-2-naphthylcarboxamide;6-Bromo-N-methyl-2-phthalenecarboxamide;6-Bromo-N-methyl-2-naphthalenecarboxamide;6-bromo-N-methylnaphthalene-2-carboxamide;2-Naphthalenecarboxamide, 6-bromo-N-methyl-
CBNumber:
CB52489907
Molecular Formula:
C12H10BrNO
Molecular Weight:
264.12
MDL Number:
MFCD14708203
MOL File:
426219-35-4.mol
MSDS File:
SDS
Last updated:2026-05-28 02:04:50

6-Bromo-N-methyl-2-naphthalenecarboxamide Properties

Boiling point 465.9±18.0 °C(Predicted)
Density 1.466
storage temp. Sealed in dry,Room Temperature
pka 14.62±0.46(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H317
Precautionary statements  P261-P272-P280-P302+P352-P333+P313-P321-P363-P501

6-Bromo-N-methyl-2-naphthalenecarboxamide price More Price(13)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
aablocks AA00BXCU 6-Bromo-N-Methyl-2-Naphthamide 99% 426219-35-4 1g $613 2026-05-28 Buy
ACHEMBLOCK T97434 6-bromo-N-methyl-2-naphthamide 95% 426219-35-4 1G $330 2026-05-27 Buy
ACHEMBLOCK T97434 6-bromo-N-methyl-2-naphthamide 95% 426219-35-4 5G $1005 2026-05-27 Buy
ACHEMBLOCK T97434 6-bromo-N-methyl-2-naphthamide 95% 426219-35-4 25G $4020 2026-05-27 Buy
Crysdot CD12072508 6-Bromo-N-methyl-2-naphthamide 98% 426219-35-4 5g $554 2026-05-27 Buy
Product number Packaging Price Buy
AA00BXCU 1g $613 Buy
T97434 1G $330 Buy
T97434 5G $1005 Buy
T97434 25G $4020 Buy
CD12072508 5g $554 Buy

6-Bromo-N-methyl-2-naphthalenecarboxamide Chemical Properties, Uses, Production

Uses

6-Bromo-N-methyl-2-naphthamide is used as a reactant in the synthesis process for orteronel (TAK-700), a potenital inhibitor that could be used for the treatment of prostate cancer.

Synthesis

6-Bromo-2-naphthoic acid

5773-80-8

Methylamine

74-89-5

6-Bromo-N-methyl-2-naphthalenecarboxamide

426219-35-4

1. 6-Bromo-2-naphthoic acid (10.1 g, 40.1 mmol) and N,N-dimethylformamide (4.75 g, 65.0 mmol) were dissolved in toluene (80 mL). 2. Thionyl chloride (5.7 g, 48.2 mmol) was slowly added dropwise to the reaction mixture at 45 to 50 °C with continuous stirring for 1 hour and then cooled to room temperature. 3. In another vessel, a solution was prepared by dissolving triethylamine (11.4 g, 112.4 mmol) and 40% methylamine methanol solution (8.1 g, 104.4 mmol) in toluene (80 mL). 4. The reaction mixture from step 2 was slowly added dropwise to the solution prepared in step 3 at 10 to 25°C with stirring for 1 hour at room temperature. 5. Water (50 mL) was added dropwise to the reaction mixture and stirring was continued at room temperature. 6. The crystals formed were collected by filtration and washed with a solvent mixture of methanol/water (2:8) (25 mL) to obtain wet crystals. 7. Dissolve the wet crystals in N,N-dimethylacetamide (70 mL) and heat to 60 °C to dissolve completely. 8. After cooling to room temperature, water (140 mL) was added slowly and dropwise to the reaction mixture. 9. The crystals were collected by filtration and washed with water (80 mL) to obtain wet crystals. 10. Suspend the wet crystals in ethyl acetate (25 mL) and stir at room temperature. 11. The crystals were collected by filtration and washed with ethyl acetate (5 mL). 12. The resulting wet crystals were dried under reduced pressure to afford 6-bromo-N-methyl-2-naphthalenecarboxamide (9.4 g, 35.6 mmol) in 89% yield. 13. 13. Product characterization: 1H NMR (500 MHz, DMSO-d6) δ 2.84 (d, J = 4.4 Hz, 3H), 7.71 (dd, J = 8.8, 2.2 Hz, 1H), 7.93-8.03 (m, 3H), 8.28 (d, J = 1.9 Hz, 1H), 8.44 (s, 1H), 8.62 (d, J = 4.1 Hz, 1H). 4.1 Hz, 1H); HRMS (ESI) m/z Calculated C12H11BrNO [M + H]+: 264.0024, measured: 264.0019; Elemental Analysis Calculated C12H10NOBr: C, 54.57; H, 3.82; N, 5.30; Br, 30.25; Measured C, 54.56; H, 3.70; N, 5.25. 3.70; N, 5.34; Br, 30.23.

References

[1] Patent: WO2012/173280, 2012, A1. Location in patent: Page/Page column 32-33
[2] Bioorganic and Medicinal Chemistry, 2011, vol. 19, # 21, p. 6356 - 6374
[3] Patent: EP1471056, 2004, A1. Location in patent: Page 32

6-Bromo-N-methyl-2-naphthalenecarboxamide Preparation Products And Raw materials

Global Suppliers ( 66)
Supplier Tel Email Country ProdList Advantage
Tetranov Biopharm 13526569071 sales@leadmedpharm.com China 7881 64
Nanjing Vital Chemical Co., Ltd. Please Send Email 18652950785 chemweiao@163.com China 4368 65
Wuhan ariel chemical Co., LTD. 18986259541 18986259541 sales@3stc.com China 3829 58
Shanghai T&W Pharmaceutical Co., Ltd. +86 21 61551611 China 9874 58
Nanjing Norris-Pharm Technology Co., Ltd 13901585132 sales@norris-pharm.com China 8869 55
SynAsst Chemical. 021-60343070 China 12731 55
Wuhan Kaymke Chemical Co., Ltd., 027-87342388 18086026008 sales@kaymke.com China 3537 55
Huainan Kedi Chemical Factory 0554-2106669 sales1@kedichem.com China 4914 55
Chengdu HuaXia Chemical Reagent Co. Ltd 400-1166-196 13458535857 cdhxsj@163.com China 13323 58
Shanghai YuLue Chemical Co., Ltd. 021-60345187 13671753212 lzz841106@aliyun.com China 10244 55

View Latest Price from 6-Bromo-N-methyl-2-naphthalenecarboxamide manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
6-Bromo-N-methyl-2-naphthalenecarboxamide pictures 2020-01-09 6-Bromo-N-methyl-2-naphthalenecarboxamide
426219-35-4
$1.00 1KG 95%-99% 1ton Career Henan Chemical Co
6-Bromo-N-methyl-2-naphthalenecarboxamide 6-bromo-N-methyl-2-naphthamide 6-BROMO-N-METHYL-2-NAPHTOAMIDE 6-Bromo-N-methyl-2-phthalenecarboxamide 2-Naphthalenecarboxamide, 6-bromo-N-methyl- 6-bromo-N-methylnaphthalene-2-carboxamide 6-Bromo-N-methyl-2-naphthylcarboxamide 426219-35-4 Naphthalene series