Benzylamine → 2-Amino-3-cyano-4-benzylamino-6-morpholino-quinoline

HRID 1715799Notes

Reaction equation

HRID 1715799 reaction equation
[NH2:1][C:2]1[C:11]([C:12]#[N:13])=[C:10](Cl)[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N:15]3[CH2:20][CH2:19][O:18][CH2:17][CH2:16]3)[CH:8]=2)[N:3]=1.[CH2:21]([NH2:28])[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>O>[NH2:1][C:2]1[C:11]([C:12]#[N:13])=[C:10]([NH:28][CH2:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N:15]3[CH2:20][CH2:19][O:18][CH2:17][CH2:16]3)[CH:8]=2)[N:3]=1

Participants

4

Reactant 2

HCID 7504BenzylamineHCID 668504532-Amino-3-cyano-4-chloro-6-(morpholin-4-yl)quinoline

Product 1

HCID 116748882-Amino-3-cyano-4-benzylamino-6-morpholino-quinoline

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

3 g of 2-amino-3-cyano-4-chloro-6-(morpholin-4-yl)quinoline and 6 mL of benzylamine are stirred at 125° C. for 3 hours. The reaction mixture is poured onto 30 mL of water. The precipitated material is filtered off, washed with 20 mL of water. After drying 2.3 g of the title compound is obtained, m.p.: 202° C.

Workup

  1. filtrationThe precipitated material is filtered off
  2. washwashed with 20 mL of water
  3. dry with materialAfter drying 2.3 g of the title compound
  4. customis obtained

Sources & evidence

ORD record
ord-3e8311c0c29e42c595705895427b76e7
Source dataset
uspto-grants-2010_09
Patent number
US07799922B2

Reaction notes

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