4-Methylmorpholine → HCID 10114657, compound

HRID 1934939Notes

Reaction equation

HRID 1934939 reaction equation
ClC(OCC(C)C)=O.CN1CCOCC1.[CH3:16][N:17]([CH3:24])[CH2:18][C:19]#[C:20][C:21](O)=[O:22].[NH2:25][C:26]1[CH:27]=[C:28]2[C:33](=[CH:34][CH:35]=1)[N:32]=[CH:31][C:30]([C:36]#[N:37])=[C:29]2[NH:38][C:39]1[CH:44]=[CH:43][CH:42]=[C:41]([Br:45])[CH:40]=1>O1CCCC1.N1C=CC=CC=1>[Br:45][C:41]1[CH:40]=[C:39]([NH:38][C:29]2[C:28]3[C:33](=[CH:34][CH:35]=[C:26]([NH:25][C:21](=[O:22])[C:20]#[C:19][CH2:18][N:17]([CH3:24])[CH3:16])[CH:27]=3)[N:32]=[CH:31][C:30]=2[C:36]#[N:37])[CH:44]=[CH:43][CH:42]=1

Participants

7

Procedure

Isobutyl chloroformate (0.260 g, 1.91 mmol) and N-methylmorpholine (0.594 g, 5.88 mmol) were added to an ice cold solution of 0.370 g (2.94 mmol) of 4-dimethylamino-2-butynoic acid in 50 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 0.144 g (21%) of yellow solid; ESMS m/z 448.0 (M+H+); mp 114-118° C.

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-382febb4b27f4e55a084c0d04decf24e
Source dataset
uspto-grants-2002_05
Patent number
US06384051B1

Reaction notes

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