Hydrochloric Acid → HCID 70011441, compound

HRID 1368908Notes

Reaction equation

HRID 1368908 reaction equation
FC(F)(F)C(O)=O.[N+:8]([C:11]1[CH:12]=[C:13]([CH:17]([NH:22][C:23](=[O:40])[CH2:24][NH:25][C:26](=[O:39])[CH2:27][CH2:28][CH2:29][CH2:30][NH:31][C:32]2[CH:37]=[C:36]([CH3:38])[CH:35]=[CH:34][N:33]=2)[CH2:18][C:19]([OH:21])=[O:20])[CH:14]=[CH:15][CH:16]=1)([O-:10])=[O:9].[ClH:41]>O>[ClH:41].[N+:8]([C:11]1[CH:12]=[C:13]([CH:17]([NH:22][C:23](=[O:40])[CH2:24][NH:25][C:26](=[O:39])[CH2:27][CH2:28][CH2:29][CH2:30][NH:31][C:32]2[CH:37]=[C:36]([CH3:38])[CH:35]=[CH:34][N:33]=2)[CH2:18][C:19]([OH:21])=[O:20])[CH:14]=[CH:15][CH:16]=1)([O-:10])=[O:9]

Participants

4

Procedure

1 mmol of 3-(3-nitrophenyl)-3-{2-[5-(4-methylpyridin-2-ylamino)pentanoylamino]acetylamino}propionic acid trifluoroacetate from Example 6 is dissolved in 10 ml of water, and 0.1% HCl solution is added dropwise. The solution is freeze dried. The procedure is repeated several times. 3-(3-nitrophenyl)-3-{2-[5-(4-methylpyridin-2-ylamino)pentanoylamino]acetylamino}propionic acid hydrochloride is obtained, RT* 17.53 min, FAB-MS (M+H)+ 458.

Workup

  1. customdried

Sources & evidence

ORD record
ord-8c8f10ae6d9c4d93b9fa05ff11e39479
Source dataset
uspto-grants-2003_06
Patent number
US06576637B1

Reaction notes

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