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Diisopropylethylamine → 4-[(2-Methoxy-ethyl)-methyl-amino]-but-2-enoic Acid[4-(3-chloro-4-fluoro-phenylamino)-3-cyano-7-methoxy-quinolin-6-yl]-amide Dihydrochloride

HRID 379163
Notes
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Reaction equation

HRID 379163 reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[O:12][CH3:13])[N:8]=[CH:7][C:6]([C:14]#[N:15])=[C:5]2[NH:16][C:17]1[CH:22]=[CH:21][C:20]([F:23])=[C:19]([Cl:24])[CH:18]=1.C(N(C(C)C)CC)(C)C.Br[CH2:35]/[CH:36]=[CH:37]/[C:38]([Cl:40])=[O:39].[CH3:41][O:42][CH2:43][CH2:44][NH:45][CH3:46].C(=O)(O)[O-].[Na+]>O1CCCC1>[ClH:24].[ClH:40].[Cl:24][C:19]1[CH:18]=[C:17]([NH:16][C:5]2[C:4]3[C:9](=[CH:10][C:11]([O:12][CH3:13])=[C:2]([NH:1][C:38](=[O:39])[CH:37]=[CH:36][CH2:35][N:45]([CH2:44][CH2:43][O:42][CH3:41])[CH3:46])[CH:3]=3)[N:8]=[CH:7][C:6]=2[C:14]#[N:15])[CH:22]=[CH:21][C:20]=1[F:23]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 5

HCID 81531DiisopropylethylamineHCID 300977(2-Methoxyethyl)(methyl)amineHCID 516892Sodium BicarbonateHCID 111424366-Amino-4-(3-chloro-4-fluoro-phenylamino)-7-methoxy-quinoline-3-carbonitrileHCID 11263885(E)-4-Bromo-2-butenoyl Chloride

Product 1

HCID 67202828
4-[(2-Methoxy-ethyl)-methyl-amino]-but-2-enoic Acid[4-(3-chloro-4-fluoro-phenylamino)-3-cyano-7-methoxy-quinolin-6-yl]-amide Dihydrochloride

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

To a stirring solution of 1.2 g (3.5 mmol) of 6-amino-4-(3-chloro-4-fluoro-phenylamino)-7-methoxy-quinoline-3-carbonitrile and 0.52 g (4.0 mmol) of diisopropylethylamine in 40 ml of tetrahydrofuran at 0° C. was added a solution of 4-bromo crotonyl chloride in 10 ml of tetrahydrofuran. After 45 min, 1.87 (21 mmol) of 2-methoxyethyl methyl amine was added. After 1 hr at room temperature, the mixture was poured into a solution of sodium bicarbonate and extracted with ethyl acetate. The organic solution was dried over magnesium sulfate. The solvent was removed and the residue was purified by chromatography on silica gel. Product eluted with ethyl acetate-methanol-triethylamine 40:8:1 giving 0.87 g of the free base. This was dissolved in 20 ml of ethyl acetate and 10 ml of a solution of hydrogen chloride in ether was added. The solid was collected giving 1.02 g of the title compound as a yellow powder: mass spectrum (electrospray, m/e): M+H 498.0, (M+2H)+2248.5.

Workup

  1. waitAfter 1 hr at room temperature
  2. extractionextracted with ethyl acetate
  3. dry with materialThe organic solution was dried over magnesium sulfate
  4. customThe solvent was removed
  5. customthe residue was purified by chromatography on silica gel
  6. washProduct eluted with ethyl acetate-methanol-triethylamine 40:8:1 giving 0.87 g of the free base
  7. dissolutionThis was dissolved in 20 ml of ethyl acetate
  8. addition10 ml of a solution of hydrogen chloride in ether was added
  9. customThe solid was collected

Sources & evidence

ORD record
ord-85cdb1c000c545b89733c9f41b8611b7
Source dataset
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06297258B1

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes