Hydrochloric Acid → HCID 86656652, compound

HRID 882909Notes

Reaction equation

HRID 882909 reaction equation
[OH-].[Li+].FC(F)(F)C([O-])=O.[NH2:10][C:11]1[C:12]([C:19]([NH:21][CH2:22][CH2:23][N+:24]([CH2:47][C:48]([O:50]C)=[O:49])([CH2:36][CH2:37][CH2:38][C:39]2[CH:44]=[CH:43][C:42]([O:45][CH3:46])=[CH:41][CH:40]=2)[CH2:25][CH2:26][CH2:27][C:28]2[CH:33]=[CH:32][C:31]([O:34][CH3:35])=[CH:30][CH:29]=2)=[O:20])=[N:13][C:14]([Cl:18])=[C:15]([NH2:17])[N:16]=1.Cl>CO>[Cl-:18].[C:48]([CH2:47][N+:24]([CH2:23][CH2:22][NH:21][C:19]([C:12]1[C:11]([NH2:10])=[N:16][C:15]([NH2:17])=[C:14]([Cl:18])[N:13]=1)=[O:20])([CH2:36][CH2:37][CH2:38][C:39]1[CH:44]=[CH:43][C:42]([O:45][CH3:46])=[CH:41][CH:40]=1)[CH2:25][CH2:26][CH2:27][C:28]1[CH:29]=[CH:30][C:31]([O:34][CH3:35])=[CH:32][CH:33]=1)([OH:50])=[O:49]

Participants

5

Procedure

Lithium hydroxide (12 mg, 0.28 mmol) is added to a stirred suspension of {2-[(3,5-Diamino-6-chloro-pyrazine-2-carbonyl)-amino]-ethyl}-methoxycarbonylmethyl-bis-[3-(4-methoxy-phenyl)-propyl]-ammonium trifluoroacetate (Example 24) (113 mg, 0.16 mmol) in methanol (9 mL), and the resulting solution is stirred at RT for 3 days. After this time the pH of the solution is adjusted to 1 using 1 N HCl solution, and the solvent then removed in vacuo. The residue is washed with water (10 mL), and dried in vacuo to yield the title compound as an orange solid. M+ 585.

Workup

  1. customthe solvent then removed in vacuo
  2. washThe residue is washed with water (10 mL)
  3. customdried in vacuo

Sources & evidence

ORD record
ord-85bc732ecdd84a35abdf7d1a1e16821a
Source dataset
uspto-grants-2012_08
Patent number
US08236808B2

Reaction notes

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