4-Methylmorpholine → HCID 86595017, compound

HRID 2121612Notes

Reaction equation

HRID 2121612 reaction equation
[NH2:1][CH2:2][CH2:3][NH:4][C:5]1[C:10]2=[N:11][N:12]([CH3:22])[C:13]([C:14]3[C:19]([Cl:20])=[CH:18][CH:17]=[CH:16][C:15]=3[Cl:21])=[C:9]2[N:8]=[C:7]([CH3:23])[N:6]=1.CN1CC[O:28]CC1.[CH2:31]([O:33][C:34]1[CH:39]=[CH:38][C:37](CC(O)=O)=[CH:36][C:35]=1[O:44][CH3:45])[CH3:32].O=C1N(P(Cl)(N2CCOC2=O)=O)CCO1>CN(C)C(=O)C.CCOC(C)=O>[Cl:20][C:19]1[CH:18]=[CH:17][CH:16]=[C:15]([Cl:21])[C:14]=1[C:13]1[N:12]([CH3:22])[N:11]=[C:10]2[C:9]=1[N:8]=[C:7]([CH3:23])[N:6]=[C:5]2[NH:4][CH:3]([C:37]1[CH:38]=[CH:39][C:34]([O:33][CH2:31][CH3:32])=[C:35]([O:44][CH3:45])[CH:36]=1)[C:2]([NH2:1])=[O:28]

Participants

7

Procedure

To a stirred solution of (2-aminoethyl)[3-(2,6-dichlorophenyl)-2,5-dimethylpyrazolo[3,4-e]pyrimidin-7-yl]amine (175 mg, 0.5 mmol) in N,N-dimethylacetamide (5 mL), add 4-methylmorpholine (101 mg, 1.0 mmol), 2-(4-ethoxy-3-methoxyphenyl)acetic acid (115 mg, 0.55 mmol) and bis(2-oxo-3-oxazolidinyl)phosphinic chloride (331 mg, 0.75 mmol). Stir the reaction mixture at ambient temperature for 14 h and dilute with EtOAc (15 mL). Wash the organic extracts successively with water (10 mL), brine (10 mL), saturated NH4Cl (10 mL), 2N NaOH (10 mL), brine (10 mL), dry over MgSO4 and evaporate under reduced pressure to obtain the title compound.

Workup

  1. washWash the organic extracts successively with water (10 mL), brine (10 mL), saturated NH4Cl (10 mL), 2N NaOH (10 mL), brine (10 mL)
  2. dry with materialdry over MgSO4
  3. customevaporate under reduced pressure

Sources & evidence

ORD record
ord-29fd8f908fa148eaa8f3fe0d7843cb0d
Source dataset
uspto-grants-2004_02
Patent number
US06696445B2

Reaction notes

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