Hydrochloric Acid → HCID 69200327, compound

HRID 746382Notes

Reaction equation

HRID 746382 reaction equation
[Cl:1][C:2]1[N:3]([CH2:33][C:34]#[C:35][CH3:36])[C:4]([C:11]([N:13]([CH2:22][C:23]2[CH:32]=[CH:31][C:30]3[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=3)[N:24]=2)[NH:14]C(OC(C)(C)C)=O)=[O:12])=[C:5]([C:7]([O:9]C)=O)[N:6]=1.Cl>C(OCC)(=O)C.O1CCOCC1>[CH2:33]([N:3]1[C:4]2[C:11](=[O:12])[N:13]([CH2:22][C:23]3[CH:32]=[CH:31][C:30]4[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=4)[N:24]=3)[NH:14][C:7](=[O:9])[C:5]=2[N:6]=[C:2]1[Cl:1])[C:34]#[C:35][CH3:36]

Participants

5

Conditions

Temperature
50 °C

Procedure

2.80 g methyl 2-chloro-5-[N′-tert-butoxycarbonyl-N-(quinolin-2-ylmethyl)-hydrazinocarbonyl]-1-(but-2-ynyl)-1H-imidazol-4-carboxylate are dissolved in 50 ml of ethyl acetate. Then 1.5 ml of 4 M hydrochloric acid in dioxane are added, and the solution is stirred for 2 h at 50° C. Then the solution is cooled to ambient temperature, the precipitate formed is separated off, washed with ethyl acetate and diethyl ether and dried in the drying cupboard at 50° C.

Workup

  1. temperatureThen the solution is cooled to ambient temperature
  2. customthe precipitate formed
  3. customis separated off
  4. washwashed with ethyl acetate and diethyl ether
  5. customdried in the drying cupboard at 50° C.

Sources & evidence

ORD record
ord-aab491655b5d4278b1afbed5d1d9d88a
Source dataset
uspto-grants-2008_07
Patent number
US07393847B2

Reaction notes

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