Hydrochloric Acid → HCID 68413743, compound

HRID 2070181Notes

Reaction equation

HRID 2070181 reaction equation
[NH2:1][C:2]([CH3:39])([CH3:38])[C:3]([NH:5][C@H:6]([CH2:34][CH:35]([CH3:37])[CH3:36])[C:7]([NH:9][CH:10]1[CH2:19][C:18]2[C:13](=[C:14]([N:20]3[C:24](=[O:25])[CH2:23][CH2:22][C:21]3=[O:26])[CH:15]=[CH:16][CH:17]=2)[N:12]([CH2:27][C:28]2[CH:32]=[CH:31][S:30][CH:29]=2)[C:11]1=[O:33])=[O:8])=[O:4].[ClH:40]>C(O)C>[ClH:40].[NH2:1][C:2]([CH3:38])([CH3:39])[C:3]([NH:5][C@H:6]([CH2:34][CH:35]([CH3:36])[CH3:37])[C:7]([NH:9][CH:10]1[CH2:19][C:18]2[C:13](=[C:14]([N:20]3[C:21](=[O:26])[CH2:22][CH2:23][C:24]3=[O:25])[CH:15]=[CH:16][CH:17]=2)[N:12]([CH2:27][C:28]2[CH:32]=[CH:31][S:30][CH:29]=2)[C:11]1=[O:33])=[O:8])=[O:4]

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 59620347HCID 59620347, compound

Product 1

HCID 68413743HCID 68413743, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

(2R)-2-(2-Amino-2-methylpropanamido)-N-(8-(2,5-dioxopyrrolidin-1-yl)-2-oxo-1-(thiophen-3-ylmethyl)-1,2,3,4-tetrahydroquinolin-3-yl)-4-methylpentanamide (14 mg) was dissolved in ethanol (1 mL), and concentrated hydrochloric acid (35% aqueous hydrochloric acid solution) (25 μL) was added thereto. The solvent was evaporated under reduced pressure, whereby the title compound (16 mg) was yielded.

Workup

  1. customThe solvent was evaporated under reduced pressure, whereby the title compound (16 mg)
  2. customwas yielded

Sources & evidence

ORD record
ord-ee2895e31b5b494ab64a0502d7bf53a3
Source dataset
uspto-grants-2012_10
Patent number
US08299255B2

Reaction notes

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