Hydrochloric Acid → HCID 68956421, compound

HRID 539402Notes

Reaction equation

O1CCCC1.[NH:6]1[CH:10]=[CH:9][N:8]=[C:7]1[CH2:11][CH:12]([CH2:43][C:44]1[NH:45][CH:46]=[CH:47][N:48]=1)[CH2:13][NH:14][C:15]([C:17]1[CH:42]=[CH:41][C:20]([CH2:21][N:22]2[CH:26]([C:27]([O:29]CC)=[O:28])[CH2:25][C:24]3([CH2:36][CH2:35][N:34]([CH2:37][CH:38]([CH3:40])[CH3:39])[CH2:33][CH2:32]3)[CH2:23]2)=[CH:19][CH:18]=1)=[O:16].[OH-].[Na+].Cl>CO>[NH:6]1[CH:10]=[CH:9][N:8]=[C:7]1[CH2:11][CH:12]([CH2:43][C:44]1[NH:45][CH:46]=[CH:47][N:48]=1)[CH2:13][NH:14][C:15]([C:17]1[CH:18]=[CH:19][C:20]([CH2:21][N:22]2[CH:26]([C:27]([OH:29])=[O:28])[CH2:25][C:24]3([CH2:32][CH2:33][N:34]([CH2:37][CH:38]([CH3:39])[CH3:40])[CH2:35][CH2:36]3)[CH2:23]2)=[CH:41][CH:42]=1)=[O:16]

Participants

Conditions

Temperature: 50 °C

Procedure

To a tetrahydrofuran (2 mL)-methanol (2 mL) solution of the compound (51 mg) produced in Example 80(3), an aqueous 2N sodium hydroxide solution (0.5 mL) was added. The reaction solution was stirred at 50° C. for 3 hours. To the reaction solution, 1N hydrochloric acid was added so as to adjust the pH to about 5. The reaction solution was concentrated under reduced pressure. The residue was washed with ethanol. An insoluble salt was removed by filtration, and then the filtrate was concentrated. The residue was purified by silica gel chromatography (dichloromethane:methanol:28% aqueous ammonia=8:2:0.5) to obtain the title compound (35 mg) having the following physical properties.

Workup

concentrationThe reaction solution was concentrated under reduced pressure
washThe residue was washed with ethanol
customAn insoluble salt was removed by filtration
concentrationthe filtrate was concentrated
customThe residue was purified by silica gel chromatography (dichloromethane:methanol:28% aqueous ammonia=8:2:0.5)

Sources & evidence

ORD record: ord-c852357ec6504da79f6b84a550e1f3d3
Source dataset: uspto-grants-2014_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08871210B2

Reaction notes

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