Hydrochloric Acid → HCID 19602827, compound

HRID 1604332Notes

Reaction equation

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

Participants

Reactant 2

HCID 313Hydrochloric Acid

HCID 19602717HCID 19602717, compound

Product 1

HCID 19602827HCID 19602827, compound

Procedure

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

Sources & evidence

ORD record: ord-45de8f2af8d94d8395aadf3d902a9ae6
Source dataset: uspto-grants-1999_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05994356

Reaction notes

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