Diisopropylethylamine → HCID 86663257, compound

HRID 2070814Notes

Reaction equation

HRID 2070814 reaction equation
[Cl:1][CH2:2][CH2:3][O:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[C:11]([NH:14][C:15]1[C:16](=[O:32])[N:17]([C:21]2[CH:22]=[C:23]([CH:27]=[C:28]([F:31])[C:29]=2[CH3:30])[C:24]([OH:26])=O)[CH:18]=[CH:19][N:20]=1)([CH3:13])[CH3:12].F[B-](F)(F)F.[N:38]1([O:47][C:48](N(C)C)=[N+](C)C)C2C=CC=CC=2N=N1.C(N(CC)C(C)C)(C)C.Cl.CON>CN(C=O)C.O>[Cl:1][CH2:2][CH2:3][O:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[C:11]([NH:14][C:15]1[C:16](=[O:32])[N:17]([C:21]2[CH:22]=[C:23]([CH:27]=[C:28]([F:31])[C:29]=2[CH3:30])[C:24]([NH:38][O:47][CH3:48])=[O:26])[CH:18]=[CH:19][N:20]=1)([CH3:12])[CH3:13]

Participants

7

Procedure

To 3-[3-({1-[2-(2-chloroethoxy)phenyl]-1-methylethyl}amino)-2-oxopyrazin-1(2H)-yl]-5-fluoro-4-methylbenzoic acid (Example 316c, 0.13 g) in DMF (3 mL) was added O-(Benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (TBTU) (0.182 g) and N,N-diisopropylethylamine (0.148 mL). The reaction was stirred for 15 min, then O-methylhydroxylamine hydrochloride (0.047 g) was added. The reaction mixture was stirred at room temperature overnight, then diluted with water and extracted with ethyl acetate. The organic layer was dried (MgSO4), filtered and evaporated to afford the subtitle compound (0.13 g).

Workup

  1. stirringThe reaction mixture was stirred at room temperature overnight
  2. extractionextracted with ethyl acetate
  3. dry with materialThe organic layer was dried (MgSO4)
  4. filtrationfiltered
  5. customevaporated

Sources & evidence

ORD record
ord-76176946fbab47c4a6085ec61c502f17
Source dataset
uspto-grants-2012_10
Patent number
US08299246B2

Reaction notes

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