Hydrochloric Acid → HCID 68412886, compound

HRID 1887759Notes

Reaction equation

HRID 1887759 reaction equation
[NH2:1][C:2]([CH3:45])([CH3:44])[C:3]([NH:5][C@H:6]([CH2:33][C:34]1[C:42]2[C:37](=[CH:38][CH:39]=[CH:40][CH:41]=2)[N:36]([CH3:43])[CH:35]=1)[C:7](=[O:32])[NH:8][CH:9]1[CH2:18][C:17]2[C:12](=[C:13]([N:19]3[CH2:23][CH2:22][CH2:21][C:20]3=[O:24])[CH:14]=[CH:15][CH:16]=2)[N:11]([CH2:25][C:26]2[CH:30]=[CH:29][S:28][CH:27]=2)[C:10]1=[O:31])=[O:4].[ClH:46]>C(O)C>[ClH:46].[NH2:1][C:2]([CH3:45])([CH3:44])[C:3]([NH:5][C@H:6]([CH2:33][C:34]1[C:42]2[C:37](=[CH:38][CH:39]=[CH:40][CH:41]=2)[N:36]([CH3:43])[CH:35]=1)[C:7](=[O:32])[NH:8][CH:9]1[CH2:18][C:17]2[C:12](=[C:13]([N:19]3[CH2:23][CH2:22][CH2:21][C:20]3=[O:24])[CH:14]=[CH:15][CH:16]=2)[N:11]([CH2:25][C:26]2[CH:30]=[CH:29][S:28][CH:27]=2)[C:10]1=[O:31])=[O:4]

Participants

4

Procedure

2-Amino-2-methyl-N-[(2R)-3-(1-methyl-1H-indol-3-yl)-1-oxo-1-[2-oxo-8-(2-oxopyrrolidin-1-yl)-1-(thiophen-3-ylmethyl)-1,2,3,4-tetrahydroquinolin-3-ylamino]propan-2-yl]propanamide (116 mg) was dissolved in ethanol (1.0 mL), and 1N hydrochloric acid (161 μL) was added thereto. Subsequently, the solvent was evaporated under reduced pressure, whereby the title compound (103 mg) was yielded.

Workup

  1. customSubsequently, the solvent was evaporated under reduced pressure, whereby the title compound (103 mg)
  2. customwas yielded

Sources & evidence

ORD record
ord-29324d5e1a664ad0bf2a09916d38cfd1
Source dataset
uspto-grants-2013_08
Patent number
US08501772B2

Reaction notes

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