Diisopropylethylamine → HCID 68283908, compound

HRID 1052123Notes

Reaction equation

HRID 1052123 reaction equation
Cl.[CH2:2]([O:5][C:6]([C@@H:8]1[CH2:13][C@@H:12]2[C@@H:10]([CH2:11]2)[N:9]1[C:14]([OH:16])=O)=[O:7])[CH:3]=[CH2:4].[C:17]([C:20]1[C:28]2[C:23](=[N:24][CH:25]=[CH:26][CH:27]=2)[N:22]([CH2:29]C(O)=O)[N:21]=1)(=[O:19])[CH3:18].CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C>CN(C=O)C>[CH2:2]([O:5][C:6]([C@@H:8]1[CH2:13][C@@H:12]2[C@@H:10]([CH2:11]2)[N:9]1[C:14](=[O:16])[CH2:29][N:22]1[C:23]2=[N:24][CH:25]=[CH:26][CH:27]=[C:28]2[C:20]([C:17](=[O:19])[CH3:18])=[N:21]1)=[O:7])[CH:3]=[CH2:4]

Participants

6

Procedure

To a solution of (1R,3S,5R)-2-azabicyclo[3.1.0]hexane-2,3-dicarboxylic acid 3-allyl ester hydrochloride (1.03 g, 6.43 mmol), (3-acetyl-pyrazolo[3,4-b]pyridin-1-yl)-acetic acid (prepared as described in Part A, 1.3 g, 5.93 mmol) and HBTU (2.70 g, 7.12 mmol) in DMF (19.7 mL) was added DIPEA (3.11 mL, 17.8 mmol). The reaction mixture was stirred for 16 h at RT. DMF was evaporated. The residue was poured into NH4Cl (sat. aq. solution) and extracted with EtOAc (3×50 mL). The organic layers were combined, dried over Na2SO4, filtered and concentrated. The crude residue was purified by flash column chromatography on silica gel (c-hexane to c-hexane/EtOAc 0:10) to give the title compound. Rf, TLC (EtOAc)=0.6; MS (LCMS): 369.0 [M+H]+, 391.0 [MH+Na]+; tR (HPLC conditions d): 2.78 min.

Workup

  1. customDMF was evaporated
  2. additionThe residue was poured into NH4Cl (sat. aq. solution)
  3. extractionextracted with EtOAc (3×50 mL)
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude residue was purified by flash column chromatography on silica gel (c-hexane to c-hexane/EtOAc 0:10)

Sources & evidence

ORD record
ord-307bdf1537c84d64a285ba8e3ae475c5
Source dataset
uspto-grants-2016_07
Patent number
US09388199B2

Reaction notes

Loading…