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Potassium Cation → Tert-butyl 4-(5-isopentyl-[1,2,4]triazolo[4,3-a]pyrazin-8-yl)piperazine-1-carboxylate

HRID 1224859
Notes
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Reaction equation

HRID 1224859 reaction equation
[Br:1][c:2]1[cH:3][n:4][c:5]([N:11]2[CH2:12][CH2:13][N:14]([C:17](=[O:18])[O:19][C:20]([CH3:21])([CH3:22])[CH3:23])[CH2:15][CH2:16]2)[c:6]2[n:7]1[cH:8][n:9][n:10]2.[CH2:24]([CH2:25][CH:26]([CH3:27])[CH3:28])[B:29]([OH:30])[OH:31].[CH3:115][c:116]1[cH:117][cH:118][cH:119][cH:120][cH:121]1.[K+:32].[K+:33].[O-:34][C:35]([O-:36])=[O:37].[cH:38]1[cH:39][cH:40][c:41]([P:42]([Pd:43]([P:44]([c:45]2[cH:46][cH:47][cH:48][cH:49][cH:50]2)([c:51]2[cH:52][cH:53][cH:54][cH:55][cH:56]2)[c:57]2[cH:58][cH:59][cH:60][cH:61][cH:62]2)([P:63]([c:64]2[cH:65][cH:66][cH:67][cH:68][cH:69]2)([c:70]2[cH:71][cH:72][cH:73][cH:74][cH:75]2)[c:76]2[cH:77][cH:78][cH:79][cH:80][cH:81]2)[P:82]([c:83]2[cH:84][cH:85][cH:86][cH:87][cH:88]2)([c:89]2[cH:90][cH:91][cH:92][cH:93][cH:94]2)[c:95]2[cH:96][cH:97][cH:98][cH:99][cH:100]2)([c:101]2[cH:102][cH:103][cH:104][cH:105][cH:106]2)[c:107]2[cH:108][cH:109][cH:110][cH:111][cH:112]2)[cH:113][cH:114]1>>[c:2]1([CH2:24][CH2:25][CH:26]([CH3:27])[CH3:28])[cH:3][n:4][c:5]([N:11]2[CH2:12][CH2:13][N:14]([C:17](=[O:18])[O:19][C:20]([CH3:21])([CH3:22])[CH3:23])[CH2:15][CH2:16]2)[c:6]2[n:7]1[cH:8][n:9][n:10]2
ParticipantsSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 813Potassium Cation2×HCID 1140TolueneHCID 19660Carbonate IonHCID 15061386(3-Methylbutyl)boronic acidHCID 58447004Tert-butyl 4-(5-bromo-[1,2,4]triazolo[4,3-a]pyrazin-8-yl)piperazine-1-carboxylateHCID 178420554HCID 178420554, compound

Product 1

HCID 67393351Tert-butyl 4-(5-isopentyl-[1,2,4]triazolo[4,3-a]pyrazin-8-yl)piperazine-1-carboxylate

Sources & evidence

ORD record
ord-435c14bf1c914a968a7f35502b7f82cf
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (5/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes