Ammonia → (S)-4-Methoxy-N-(3-(4-((1-(5-methyl-4-oxo-3-phenyl-3,4-dihydropyrrolo[2,1-f][1,2,4]triazin-2-yl)ethyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-5-yl)phenyl)benzenesulfonamide

HRID 1052749Notes

Reaction equation

HRID 1052749 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([NH:12][C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([C:19]3[C:27]4[C:26]([NH:28][C@H:29]([C:31]5[N:36]([C:37]6[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=6)[C:35](=[O:43])[C:34]6=[C:44]([CH3:47])[CH:45]=[CH:46][N:33]6[N:32]=5)[CH3:30])=[N:25][CH:24]=[N:23][C:22]=4[N:21](COCC[Si](C)(C)C)[CH:20]=3)[CH:14]=2)(=[O:11])=[O:10])=[CH:5][CH:4]=1.FC(F)(F)C(O)=O.N>>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([S:9]([NH:12][C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([C:19]3[C:27]4[C:26]([NH:28][C@H:29]([C:31]5[N:36]([C:37]6[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=6)[C:35](=[O:43])[C:34]6=[C:44]([CH3:47])[CH:45]=[CH:46][N:33]6[N:32]=5)[CH3:30])=[N:25][CH:24]=[N:23][C:22]=4[NH:21][CH:20]=3)[CH:14]=2)(=[O:10])=[O:11])=[CH:7][CH:8]=1

Participants

4

Procedure

(S)-4-Methoxy-N-(3-(4-((1-(5-methyl-4-oxo-3-phenyl-3,4-dihydropyrrolo[2,1-f][1,2,4]triazin-2-yl)ethyl)amino)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl)phenyl)benzenesulfonamide (25 mg, 0.02 mmol) was treated with trifluoroacetic acid (500 μl, 6.49 mmol) and a solution of ammonia (7N in methanol, 500 μl, 3.50 mmol) according to the method described in Example 27. The residue was purified using SP1® Purification System (0% to 100% n-hexane-ethyl acetate) to obtain 13 mg (86% yield) of the title compound.

Workup

  1. customThe residue was purified
  2. customSP1® Purification System (0% to 100% n-hexane-ethyl acetate)

Sources & evidence

ORD record
ord-b59abdb3f23f4d55838ad7d1251dccce
Source dataset
uspto-grants-2016_07
Patent number
US09388189B2

Reaction notes

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