1-(5-Methylpyridin-2-yl)cyclopropan-1-amine → HCID 67390164, compound
Reaction equation
[Br:105][c:106]1[cH:107][cH:108][c:109]([C:110]2([NH2:111])[CH2:112][CH2:113]2)[n:114][cH:115]1.[C:34]([O:35][C:36](=[O:37])[NH:38][CH2:39][c:40]1[cH:41][n:42][c:43]([C:44]2([NH2:45])[CH2:46][CH2:47]2)[cH:48][cH:49]1)([CH3:50])([CH3:51])[CH3:52].[C:67]([CH:68]([O:69][SiH:70]([CH3:71])[CH3:72])[c:73]1[cH:74][cH:75][c:76]([C:77]2([NH2:78])[CH2:79][CH2:80]2)[n:81][cH:82]1)([CH3:83])([CH3:84])[CH3:85].[C:86]([SiH2:87][O:88][C:89]([CH3:90])([CH3:91])[c:92]1[cH:93][cH:94][n:95][c:96]([C:97]2([NH2:98])[CH2:99][CH2:100]2)[cH:101]1)([CH3:102])([CH3:103])[CH3:104].[CH3:13][c:14]1[o:15][n:16][c:17]([C:18]2([NH2:19])[CH2:20][CH2:21]2)[cH:22]1.[CH3:140][c:141]1[s:142][cH:143][c:144]([C:145]2([NH2:146])[CH2:147][CH2:148]2)[n:149]1.[CH3:23][c:24]1[cH:25][cH:26][c:27]([C:28]2([NH2:29])[CH2:30][CH2:31]2)[n:32][cH:33]1.[CH3:53][N:54]([CH2:55][c:56]1[cH:57][cH:58][c:59]([C:60]2([NH2:61])[CH2:62][CH2:63]2)[n:64][cH:65]1)[CH3:66].[CH:1]1([c:4]2[o:5][cH:6][c:7]([C:9]3([NH2:12])[CH2:10][CH2:11]3)[n:8]2)[CH2:2][CH2:3]1.[I:116][c:117]1[cH:118][cH:119][n:120][c:121]([C:122]2([NH2:123])[CH2:124][CH2:125]2)[cH:126]1.[NH2:127][C:128]1([c:129]2[n:130][cH:131][c:132]([N:133]([CH3:134])[CH3:135])[cH:136][cH:137]2)[CH2:138][CH2:139]1>>[CH:1]([CH3:2])([CH3:3])[c:4]1[o:5][cH:6][c:7]([C:9]2([NH2:12])[CH2:10][CH2:11]2)[n:8]1Participants
12
Reactant 11
Product 1
Sources & evidence
- ORD record
- ord-05000814d0e045698651b77af92e968a
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (7/10)
Reaction notes
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