Glutaric Acid → HCID 178512828, compound

HRID 703384

Reaction equation

Cl.N(CCCCC(N)=O)C(N)=N.Cl.Cl.NCCCNCCCCNC(=O)C(O)O.C(O)(=O)CCCC(O)=O.Cl.Cl.Cl.[NH2:42][CH2:43][CH2:44][CH2:45][NH:46][CH2:47][CH2:48][CH2:49][CH2:50][NH:51][C:52](=[O:66])[CH:53]([NH:55][C:56](=[O:65])[CH2:57][CH2:58][CH2:59][CH2:60][NH:61][C:62]([NH2:64])=[NH:63])[OH:54]>O>[NH2:42][CH2:43][CH2:44][CH2:45][NH:46][CH2:47][CH2:48][CH2:49][CH2:50][NH:51][C:52](=[O:66])[CH:53]([NH:55][C:56](=[O:65])[CH2:57][CH2:58][CH2:59][CH2:60][NH:61][C:62]([NH2:64])=[NH:63])[OH:54]

Participants

Conditions

Temperature: 60 °C

Procedure

A mixture of 92.4 mg (0.48 mmole) of 5-guanidino pentanamide hydrochloride, 166.5 mg (0.57 mmole) of N-[4-(3-aminopropyl)aminobutyl]-2,2-dihydroxyethanamide dihydrochloride, 62.8 mg (0.48 mmole) of glutaric acid and 0.1 ml of water was heated at 60° C. for 24 hours. After completion of the reaction, 5 ml of water was added to the reaction mixture which was then purified in a manner similar to that in Example 1, using CM-Sephadex® C-25 (Na-type) and Sephadex® LH-20 to obtain 82.5 mg (37.1% yield) of a white powder of N-[4-(3-aminopropyl)aminobutyl]-2-(5-guanidinopentanamido)-2-hydroxyethanamide trihydrochloride.

Workup

additionwas added to the reaction mixture which
customwas then purified in a manner similar to that in Example 1

Sources & evidence

ORD record: ord-245c3b8d4f45489997d738fce95b00cb
Source dataset: uspto-grants-1991_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04983328

Linked notes

Loading…