Hydrochloric Acid → HCID 131715995, compound

HRID 231478Notes

Reaction equation

CC(C)(OC([NH:7][CH:8]([C:19]([NH:21][C@@H:22]([C:24]([NH:26][CH:27]1[C:35]2[C:30](=[CH:31][CH:32]=[CH:33][CH:34]=2)[CH2:29][CH2:28]1)=[O:25])[CH3:23])=[O:20])[CH2:9][C:10]1[C:15]([CH3:16])=[CH:14][C:13]([OH:17])=[CH:12][C:11]=1[CH3:18])=O)C.[ClH:37]>>[ClH:37].[CH3:16][C:15]1[CH:14]=[C:13]([OH:17])[CH:12]=[C:11]([CH3:18])[C:10]=1[CH2:9][CH:8]([C:19]([NH:21][C@@H:22]([C:24]([NH:26][CH:27]1[C:35]2[C:30](=[CH:31][CH:32]=[CH:33][CH:34]=2)[CH2:29][CH2:28]1)=[O:25])[CH3:23])=[O:20])[NH2:7]

Participants

Reactant 2

HCID 313Hydrochloric Acid

HCID 15702974HCID 15702974, compound

Product 1

HCID 131715995HCID 131715995, compound

Procedure

The title compound of Example 18 was deblocked and converted to its HCl salt by the method of Example 6.

Sources & evidence

ORD record: ord-5362125a959241d1a1e26f345bbf0945
Source dataset: uspto-grants-1989_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04847241

Reaction notes

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