4-Methylmorpholine → HCID 10884588, compound

HRID 1934940Notes

Reaction equation

HRID 1934940 reaction equation
ClC(OCC(C)C)=O.CN1CCOCC1.[CH3:16][O:17][CH2:18][C:19]#[C:20][C:21]([OH:23])=O.[NH2:24][C:25]1[CH:26]=[C:27]2[C:32](=[CH:33][CH:34]=1)[N:31]=[CH:30][C:29]([C:35]#[N:36])=[C:28]2[NH:37][C:38]1[CH:43]=[CH:42][CH:41]=[C:40]([Br:44])[CH:39]=1>O1CCCC1.N1C=CC=CC=1>[Br:44][C:40]1[CH:39]=[C:38]([NH:37][C:28]2[C:27]3[C:32](=[CH:33][CH:34]=[C:25]([NH:24][C:21](=[O:23])[C:20]#[C:19][CH2:18][O:17][CH3:16])[CH:26]=3)[N:31]=[CH:30][C:29]=2[C:35]#[N:36])[CH:43]=[CH:42][CH:41]=1

Participants

7

Reactant 4

HCID 79724-MethylmorpholineHCID 62365Isobutyl chloroformateHCID 99677126-Amino-4-(3-bromophenylamino)quinoline-3-carbonitrileHCID 111262132-Butynoic acid, 4-methoxy-

Product 1

HCID 10884588HCID 10884588, compoundYield 35%

Reagents, catalysts & solvents 2

HCID 1049PyridineSolventHCID 8028TetrahydrofuranSolvent

Procedure

Isobutyl chloroformate (0.410 g, 3.0 mmol) and N-methylmorpholine (0.910 g, 9.0 mmol) were added to an ice cold solution of 0.680 g (6.0 mmol) of 4-methoxy-2-butynoic acid in 20 mL of tetrahydrofuran under N2. After stirring for 30 min, a solution of 0.500 g (01.47 mmol) of 6-amino-4-[(3-bromophenyl)amino]-3-quinolinecarbonitrile in 10 mL of pyridine was added and the mixture was stirred at 0° C. for 2 h. The reaction was quenched with ice water, and then poured into saturated sodium bicarbonate and brine. The product was collected, washed with ethyl acetate, and dried in vacuo to give 0.200 g (35%) of yellow solid; ESMS m/z 435.1 (M+H+); mp 198-202° C. (dec).

Workup

  1. stirringthe mixture was stirred at 0° C. for 2 h
  2. customThe reaction was quenched with ice water
  3. additionpoured into saturated sodium bicarbonate and brine
  4. customThe product was collected
  5. washwashed with ethyl acetate
  6. customdried in vacuo

Sources & evidence

ORD record
ord-800a194199314cc4871d7e048d21b286
Source dataset
uspto-grants-2002_05
Patent number
US06384051B1

Reaction notes

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