4-BROMO-2,3-DIHYDRO-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
4-BROMO-2,3-DIHYDRO-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER Basic information
- Product Name:
- 4-BROMO-2,3-DIHYDRO-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
- Synonyms:
-
- 4-BROMO-2,3-DIHYDRO-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
- N-Boc-4-broMoindoline
- 1H-Indole-1-carboxylic acid, 4-broMo-2,3-dihydro-, 1,1-diMethylethyl ester
- tert-Butyl 4-broMoindoline-1-carboxylate
- Tert-butyl 4-bromo-2,3-dihydroindole-1-carboxylate
- CAS:
- 885272-46-8
- MF:
- C13H16BrNO2
- MW:
- 298.18
- Mol File:
- 885272-46-8.mol
4-BROMO-2,3-DIHYDRO-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER Chemical Properties
- Boiling point:
- 362.0±41.0 °C(Predicted)
- Density
- 1.400±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- pka
- -0.34±0.20(Predicted)
- Appearance
- White to yellow Solid-Liquid Mixture
- InChI
- InChI=1S/C13H16BrNO2/c1-13(2,3)17-12(16)15-8-7-9-10(14)5-4-6-11(9)15/h4-6H,7-8H2,1-3H3
- InChIKey
- DUZIJTYKDFFQDJ-UHFFFAOYSA-N
- SMILES
- N1(C(OC(C)(C)C)=O)C2=C(C(Br)=CC=C2)CC1
4-BROMO-2,3-DIHYDRO-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER Usage And Synthesis
Uses
4-BROMO-2,3-DIHYDRO-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER is an indole derivative used in pharmaceutical synthesis and scientific research.
Synthesis
24424-99-5
86626-38-2
885272-46-8
The reaction mixture was stirred overnight at room temperature in acetonitrile (8 mL) with 4-bromo-2,3-dihydro-1H-indole (759 mg, 3.81 mmol) and di-tert-butyl dicarbonate (976 mg, 4.48 mmol). After completion of the reaction, the solvent was removed by rotary evaporation and the residue was dissolved in ethyl acetate (40 mL). The organic layer was washed sequentially with water (3 x 20 mL) and saturated saline (1 x 20 mL). The organic phase was collected, dried over anhydrous sodium sulfate and concentrated under reduced pressure. Finally, it was purified by silica gel column chromatography (eluent: petroleum ether) to afford N-Boc-4-bromoindoline (840 mg, 74% yield) as a white solid.1H NMR (400 MHz, DMSO-d6) δ 1.50 (s, 9H), 3.02 (t, J = 8.8 Hz, 2H), 3.94 (t, J = 8.8 Hz, 2H) 7.12 (m, 2H), 7.56 (m, 1H).
References
[1] Patent: WO2011/130628, 2011, A1. Location in patent: Page/Page column 225
[2] Patent: US2013/102595, 2013, A1. Location in patent: Paragraph 0566
[3] Patent: JP2015/187145, 2015, A. Location in patent: Paragraph 0481
[4] Patent: WO2016/25933, 2016, A2. Location in patent: Page/Page column 185
4-BROMO-2,3-DIHYDRO-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTERSupplier
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