Hydrochloric Acid → HCID 131726872, compound

HRID 2223017Notes

Reaction equation

HRID 2223017 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-3dc9f1ad2e414d779c2bfda305690c60
Source dataset
uspto-grants-2008_05
Patent number
US07375082B2

Reaction notes

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