Acetic Acid → HCID 86708603, compound

HRID 1430901Notes

Reaction equation

HRID 1430901 reaction equation
[NH2:1][CH:2]1[CH2:7][CH2:6][N:5]([C:8]2[C:9]([Cl:31])=[C:10]([NH:16][C:17]3[N:22]=[C:21]([NH:23][CH2:24][CH3:25])[C:20]4=[N:26][CH:27]=[C:28]([C:29]#[N:30])[N:19]4[N:18]=3)[CH:11]=[C:12]([C:14]#[N:15])[CH:13]=2)[CH2:4][CH2:3]1.C(OC)(OC)OC.CC(O)=O.[O:43]1[CH2:46][C:45](=O)[CH2:44]1.C([BH3-])#N.[Na+]>C1COCC1.CO>[Cl:31][C:9]1[C:8]([N:5]2[CH2:6][CH2:7][CH:2]([NH:1][CH:45]3[CH2:46][O:43][CH2:44]3)[CH2:3][CH2:4]2)=[CH:13][C:12]([C:14]#[N:15])=[CH:11][C:10]=1[NH:16][C:17]1[N:22]=[C:21]([NH:23][CH2:24][CH3:25])[C:20]2=[N:26][CH:27]=[C:28]([C:29]#[N:30])[N:19]2[N:18]=1

Participants

8

Procedure

2-((3-(4-aminopiperidin-1-yl)-2-chloro-5-cyanophenyl)amino)-4-(ethylamino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile (Example 329) (48 mg, 0.110 mmol) was taken up in THF (2 mL) and Methanol (2 mL) and trimethyl orthoformate (0.5 mL, 4.52 mmol), AcOH (0.05 mL, 0.873 mmol) in a round bottom flask. Oxetan-3-one (0.1 mL, 1.560 mmol) were added. The reaction mixture was stirred at rt for 15 mins. sodium cyanoborohydride (50 mg, 0.796 mmol) was added and the reaction was stirred at r.t. for 2 hrs. LC/MS showed about 40% conversion to the desired product. Another batch of oxetan-3-one (0.1 mL, 1.560 mmol), trimethyl orthoformate (0.5 mL, 4.52 mmol), AcOH (0.05 mL, 0.873 mmol) and sodium cyanoborohydride (50 mg, 0.796 mmol) were added to the reaction mixture and let stirred for another 30 mins. LC/MS showed completed conversion to the product. The mixture was concentrated to almost dryness, diluted with EtOAc and washed with NaHCO3, then brine, dried over MgSO4 and concentrated. The crude was then purified by PREP-HPLC to give 21.3 mg of desired product

Workup

  1. stirringthe reaction was stirred at r.t. for 2 hrs

Sources & evidence

ORD record
ord-325ad665cd3d4da9b31bb4c43448bd7d
Source dataset
uspto-grants-2015_01
Patent number
US08940736B2

Reaction notes

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