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Merck

570907

Sigma-Aldrich

(S,S,S)-2-氮杂双环[3.3.0]辛烷-3-羧酸苄酯盐酸盐

97%

别名:

(S,S,S)-2-氮杂双环[3,3,0]辛烷羧酸苄酯 盐酸盐, (S,S,S)-2-氮杂双环[3,3,0]辛烷-3-羧酸苄酯 盐酸盐

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About This Item

经验公式(希尔记法):
C15H19NO2 ·HCl
CAS号:
分子量:
281.78
MDL號碼:
分類程式碼代碼:
12352005
PubChem物質ID:

化驗

97%

光學活性

[α]20/D -26°, c = 1% in DMSO

mp

176-180 °C (lit.)

SMILES 字串

Cl[H].[H][C@@]12CCC[C@]1([H])N[C@@H](C2)C(=O)OCc3ccccc3

InChI

1S/C15H19NO2.ClH/c17-15(18-10-11-5-2-1-3-6-11)14-9-12-7-4-8-13(12)16-14;/h1-3,5-6,12-14,16H,4,7-10H2;1H/t12-,13-,14-;/m0./s1

InChI 密鑰

HLXCXOQXUDRJLF-JKBZPBJLSA-N

應用

Benzyl (S,S,S)-2-azabicyclo[3.3.0]octane-3-carboxylate hydrochloride can be used:
  • In the preparation of ramipril, an angiotensin-converting enzyme (ACE) inhibitor.
  • As a starting material for the synthesis of octahydrocyclopenta[b]pyrrole-2-carbonitrile derivatives as potent DPP4 inhibitors.

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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Xun Ji et al.
European journal of medicinal chemistry, 86, 242-256 (2014-08-29)
Based on the previous work in our group and the principle of computer-aided drug design, a series of novel β-amino pyrrole-2-carbonitrile derivatives was designed and synthesized. Compounds 8l and 9l were efficacious and selective DPP4 inhibitors resulting in decreased blood
Expeditious synthesis of Ramipril: an Angiotensin-converting enzyme (ACE) inhibitor
Malakondaiah GC, et al.
Synthetic Communications, 38(11), 1737-1744 (2008)

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