Hydrochloric Acid → HCID 131726872, compound

HRID 32334Notes

Reaction equation

HRID 32334 reaction equation
[NH:1](C(OC(C)(C)C)=O)[CH2:2][C:3]([NH:5][CH2:6][C:7]([NH:9][C@H:10]([C:15]([OH:17])=[O:16])[CH2:11][CH:12]([CH3:14])[CH3:13])=[O:8])=[O:4].[CH3:25][N:26]1[C@@H:43]2[CH2:44][C:31]3[CH:32]=[CH:33][C:34]([O:45][CH3:46])=[C:35]4[O:36][C@H:37]5[C:38]([CH2:40][CH2:41][C@@H:42]2[C@:29]5([C:30]=34)[CH2:28][CH2:27]1)=[O:39].Cl>O1CCOCC1>[CH3:14][CH:12]([CH2:11][C@H:10]([NH:9][C:7]([CH2:6][NH:5][C:3]([CH2:2][NH2:1])=[O:4])=[O:8])[C:15]([OH:17])=[O:16])[CH3:13].[CH3:25][N:26]1[C@@H:43]2[CH2:44][C:31]3[CH:32]=[CH:33][C:34]([O:45][CH3:46])=[C:35]4[O:36][C@H:37]5[C:38]([CH2:40][CH2:41][C@@H:42]2[C@:29]5([C:30]=34)[CH2:28][CH2:27]1)=[O:39]

Participants

4

Procedure

To the Boc-Gly-Gly-Leu-Hydrocodone (2.08 g) was added 50 ml of 4N HCl in dioxane. The resulting mixture was stirred at ambient temperatures for 18 hours. Solvent was removed and final product dried under vacuum. Solid was collected as a slightly yellow solid (1.72 g, 86% yield): 1H NMR (DMSO-d6) δ 0.89 (dd, 6H), 1.50-1.87 (m, 5H), 2.26 (m, 2H), 2.66 (m, 2H), 2.82-2.97 (m, 5H), 3.21 (m, 2H), 3.60 (m, 4H), 3.88 (m, 5H), 4.37 (m, 1H), 5.04 (s, 1H), 5.60 (s, 1H), 6.79 (d, 2H), 8.07 (br s, 3H), 8.54 (br s, 1H), 8.66 (br s, 1H), 11.29 (br s, 1H).

Workup

  1. customSolvent was removed
  2. dry with materialfinal product dried under vacuum

Sources & evidence

ORD record
ord-a5925eb1168f46d4ab637789b326b86b
Source dataset
uspto-grants-2008_09
Patent number
US07427600B2

Reaction notes

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