Hydrochloric Acid → HCID 19602970, compound

HRID 1604334Notes

Reaction equation

C(OC([N:8]1[CH2:13][CH2:12][CH:11]([CH:14]([NH:33][CH2:34][C:35]2[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=2)[CH:15]2[CH2:20][CH2:19][N:18]([C:21]3[CH:26]=[CH:25][C:24]([O:27][CH2:28][C:29]([O:31][CH3:32])=[O:30])=[CH:23][CH:22]=3)[CH2:17][CH2:16]2)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:41]>>[ClH:41].[ClH:41].[CH3:32][O:31][C:29]([CH2:28][O:27][C:24]1[CH:23]=[CH:22][C:21]([N:18]2[CH2:19][CH2:20][CH:15]([CH:14]([CH:11]3[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]3)[NH:33][CH2:34][C:35]3[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=3)[CH2:16][CH2:17]2)=[CH:26][CH:25]=1)=[O:30]

Participants

Reactant 2

HCID 313Hydrochloric Acid

HCID 19602740HCID 19602740, compound

Product 1

HCID 19602970HCID 19602970, compound

Procedure

Prepared from 4-[(1-tert-butyloxycarbonylpiperidin-4-yl)-N-benzylaminomethyl]-1-(4-methoxycarbonylmethyloxyphenyl)piperidine and ethereal hydrochloric acid.

Sources & evidence

ORD record: ord-bedd56670fd949f6b6f9a7f83d06ec10
Source dataset: uspto-grants-1999_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05994356

Reaction notes

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