Hydrochloric Acid → HCID 66590088, compound

HRID 1242153Notes

Reaction equation

HRID 1242153 reaction equation
Cl.C(O[C:7](=O)[N:8]([CH:10]1[CH2:15][CH2:14][CH:13]([N:16]([C:34]([C:36]2[S:40][C:39]3[CH:41]=[CH:42][CH:43]=[CH:44][C:38]=3[C:37]=2[Cl:45])=[O:35])[CH2:17][C:18]2[CH:19]=[C:20]([C:26]3[CH:31]=[CH:30][C:29]([C:32]#[N:33])=[CH:28][CH:27]=3)[C:21]([O:24][CH3:25])=[CH:22][CH:23]=2)[CH2:12][CH2:11]1)C)(C)(C)C.C(O)C>C(OC)(C)(C)C>[ClH:45].[C:32]([C:29]1[CH:30]=[CH:31][C:26]([C:20]2[C:21]([O:24][CH3:25])=[CH:22][CH:23]=[C:18]([CH2:17][N:16]([CH:13]3[CH2:12][CH2:11][CH:10]([NH:8][CH3:7])[CH2:15][CH2:14]3)[C:34]([C:36]3[S:40][C:39]4[CH:41]=[CH:42][CH:43]=[CH:44][C:38]=4[C:37]=3[Cl:45])=[O:35])[CH:19]=2)=[CH:27][CH:28]=1)#[N:33]

Participants

5

Procedure

Concentrated hydrochloric acid (27.5 mL) was added to a solution of compound 6 (11.0 g, 17.1 mmol) and ethanol (82.5 mL). The mixture was stirred until reaction was complete as monitored by TLC. The mixture was concentrated in vacuo and dichloromethane added and concentrated again, this was repeated until a solid was obtained. The solid was then slurried with t-butylmethyl ether (30 mL), filtered, and the organic layer dried (MgSO4) and concentrated in vacuo to give the title compound 7 (10.0 g, 99%): δH (360 MHz: DMSO, 70° C.) 1.30–1.50 (m, 2H), 1.85 (br s, 4H), 2.12 (br, d, 2H), 2.48 (s, 3H), 2.91 (br t, 1H), 3.81 (s, 3H), 3.87 (br s, 1H), 4.71 (s, 2H), 7.14 (d, 1H), 7.29 (s, 1H), 7.40 (d, 1H), 7.57–7.68 (m, 4H), 7.80–7.90 (m, 3H), 8.09 (d, 1H), 8.82 (br s, 2H).

Workup

  1. concentrationThe mixture was concentrated in vacuo and dichloromethane
  2. additionadded
  3. concentrationconcentrated again
  4. customwas obtained
  5. filtrationfiltered
  6. dry with materialthe organic layer dried (MgSO4)
  7. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-2e3e9807fc684b919e2f09200b08baba
Source dataset
uspto-grants-2006_10
Patent number
US07115653B2

Reaction notes

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