Diisopropylethylamine → HCID 66706295, compound

HRID 1470579Notes

Reaction equation

HRID 1470579 reaction equation
[CH3:1][O:2][C:3](=[O:12])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([NH2:10])[C:5]=1[NH2:11].[C:13]1([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[C:14](C2C(C(O)=O)=CC=CC=2)=[CH:15][CH:16]=[CH:17][CH:18]=1.CN([C:37]([O:41]N1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(N(C(C)C)CC)(C)C>CN(C=O)C.O>[CH3:1][O:2][C:3](=[O:12])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([NH:10][C:37]([C:31]2[CH:30]=[CH:29][C:28]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)=[CH:33][CH:32]=2)=[O:41])[C:5]=1[NH2:11]

Participants

7

Procedure

To a stirred solution of 2,3-diamino-benzoic acid methyl ester (200 mg, 1.2 mmol, and biphenyl benzoic acid (238 mg, 1.2 mmol), HATU (1.14 g, 3 mmol) in dry DMF (5 mL) was added diisopropylethyl amine (0.6 mL, 3.6 mmol). The mixture was stirred at ambient temperature overnight and poured into water (50 mL). The precipitated solid was filtered and dried in a vacuum oven to afford the required compound which was used directly for the next step without any purification (300 mg, 72%).

Workup

  1. filtrationThe precipitated solid was filtered
  2. customdried in a vacuum oven

Sources & evidence

ORD record
ord-b1c3ab8a85ac4ce8a1451287aa3b6b27
Source dataset
uspto-grants-2015_04
Patent number
US09006454B2

Reaction notes

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