Basic information Safety Supplier Related

Methyl 7-aminoheptanoate hydrochloride

Basic information Safety Supplier Related

Methyl 7-aminoheptanoate hydrochloride Basic information

Product Name:
Methyl 7-aminoheptanoate hydrochloride
Synonyms:
  • Methyl 7-aminoheptanoate
  • 7-AMINOHEPTANOICMETHYLESTER
  • Methyl 7-aminoheptanoate hydrochloride 7-Amino-heptanoic acid methyl ester hydrochloride
  • Methyl 7-aminoheptanoate HCl
  • 7-Amino-heptanoic acid methyl ester
  • CHEMPACIFIC 38337
  • (7-methoxy-7-oxoheptyl)azanium
  • Heptanoic acid,7-amino-, methyl ester, hydrochloride (1:1)
CAS:
17994-94-4
MF:
C8H17NO2
MW:
159.23
EINECS:
682-559-6
Mol File:
17994-94-4.mol
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Methyl 7-aminoheptanoate hydrochloride Chemical Properties

Melting point:
119-121℃
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
White to off-white Solid
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Safety Information

HS Code 
2921199990
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Methyl 7-aminoheptanoate hydrochloride Usage And Synthesis

Uses

Methyl 7-aminoheptanoate is used in the synthesis of the antidepressant drug Amineptine (A634280).

Synthesis

67-56-1

929-17-9

17994-94-4

Thionyl chloride (1.81 mL, 24.8 mmol) was slowly added dropwise to a cooled suspension of 7-aminoheptanoic acid (1.8 g, 12.4 mmol) in methanol (30 mL) under stirring conditions, and the reaction temperature was controlled to be maintained between -5°C and -10°C. The reaction was carried out by stirring. After the thionyl chloride drop was completed, the reaction mixture was gradually warmed up to room temperature with continuous stirring overnight. Upon completion of the reaction, the solvent was removed by vacuum concentration to give a white solid product. The solid was ground twice with ether to give a final 2.38 g of 7-aminoheptanoic acid methyl ester hydrochloride (1:1) (5) as a white solid (theoretical yield 4.8 g, 100% yield).

References

[1] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 9, p. 2809 - 2812
[2] Patent: WO2011/91213, 2011, A2. Location in patent: Page/Page column 76-78
[3] Patent: WO2013/13113, 2013, A2. Location in patent: Page/Page column 72-73
[4] Journal of Medicinal Chemistry, 2006, vol. 49, # 20, p. 6094 - 6103
[5] Journal of Medicinal Chemistry, 2018, vol. 61, # 6, p. 2589 - 2603

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