N-Methyl-1-amino-hex-5-ene
N-Methyl-1-amino-hex-5-ene Basic information
- Product Name:
- N-Methyl-1-amino-hex-5-ene
- Synonyms:
-
- 5-HEXEN-1-AMINE, N-METHYL-
- N-methylhex-5-en-1-amine
- 5-Hexen-1-aMine, N-Methyl-N-Methylhex-5-en-1-aMine
- N-methyl-5-hexen-1-amine
- N-Methyl-1-amino-hex-5-ene
- N-Methylhex-5-en-1-amine,98% (stabilized with MEHQ)
- CAS:
- 55863-02-0
- MF:
- C7H15N
- MW:
- 113.2
- Mol File:
- 55863-02-0.mol
N-Methyl-1-amino-hex-5-ene Chemical Properties
- Boiling point:
- 146.5±19.0 °C(Predicted)
- Density
- 0.764±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- solubility
- Chloroform (Slightly), Methanol (Slightly)
- pka
- 10.74±0.10(Predicted)
- form
- Oil
- color
- Colourless
- Stability:
- Volatile
- InChI
- InChI=1S/C7H15N/c1-3-4-5-6-7-8-2/h3,8H,1,4-7H2,2H3
- InChIKey
- KKIMETYRXLWWSD-UHFFFAOYSA-N
- SMILES
- C(NC)CCCC=C
N-Methyl-1-amino-hex-5-ene Usage And Synthesis
Uses
N-Methylhex-5-en-1-amine can be used as a reagent to prepare quinazoline substituted cyclopentane and proline-urea based macrocycles as Hepatitis C virus (HCV) NS3/4A protease inhibitors.
Synthesis
2695-47-8
74-89-5
55863-02-0
The following step: To a reaction flask was added a methanol solution containing 25% methylamine in an amount of 10 equivalents of methylamine. Subsequently 1 equivalent of 6-bromo-1-hexene was added to the reaction flask and mixed with stirring. The reaction mixture was heated to 40°C in an oil bath and kept at this temperature for 3 hours. Upon completion of the reaction, the mixture was cooled to 20 °C and 0.1 equivalent of p-methoxyphenol was added as a stabilizer, along with 1 equivalent of sodium hydroxide. The excess methylamine methanol solution was recovered under negative pressure. Next, the mixture was heated to 50 °C and a colorless liquid product, N-methyl-5-hexen-1-amine, was obtained by distillation under reduced pressure. The yield of this step was 67% and the purity of the product was 96.5%.
References
[1] Patent: CN108003037, 2018, A. Location in patent: Paragraph 0014-0028
[2] Bulletin de la Societe Chimique de France, 1975, p. 2315 - 2320
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