Hydrochloric Acid → HCID 67288977, compound

HRID 2038400Notes

Reaction equation

HRID 2038400 reaction equation
[C:1]1([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH:6]=[CH:5][C:4]([C:7]([N:9]2[CH2:12][CH:11]([NH:13][C@H:14]3[CH2:18][CH2:17][N:16](C(OC(C)(C)C)=O)[CH2:15]3)[CH2:10]2)=[O:8])=[CH:3][CH:2]=1.Cl>CO.O1CCOCC1>[C:1]1([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH:2]=[CH:3][C:4]([C:7]([N:9]2[CH2:10][CH:11]([NH:13][C@H:14]3[CH2:18][CH2:17][NH:16][CH2:15]3)[CH2:12]2)=[O:8])=[CH:5][CH:6]=1

Participants

5

Procedure

To a solution of compound 3e (2.5 g, 5.92 mmol) in MeOH (7 mL) was added an HCl solution in dioxane (4M, 12 mL) at room temperature. The mixture was stirred at room temperature for 4 h. The solvent was removed by evaporation. Ether (30 mL) was added to the residue. The off-white solid was collected by filtration, washed with hexanes, and dried under vacuum. The crude compound 3f was used in the next reaction without further purification. MS m/z (M+H+) 322.

Workup

  1. customThe solvent was removed by evaporation
  2. additionEther (30 mL) was added to the residue
  3. filtrationThe off-white solid was collected by filtration
  4. washwashed with hexanes
  5. customdried under vacuum
  6. customThe crude compound 3f was used in the next reaction without further purification

Sources & evidence

ORD record
ord-81557b1a13e3443ca9ad85ae11a6fe53
Source dataset
uspto-grants-2013_11
Patent number
US08575363B2

Reaction notes

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