Dichloromethane → HCID 70989682, compound

HRID 1127632Notes

Reaction equation

HRID 1127632 reaction equation
[CH2:1]([CH3:2])[n:3]1[n:4][cH:5][c:6]2[c:7]1[n:8][c:9]([CH2:32][CH3:33])[c:10]([CH2:19][NH:20][C:21](=[O:22])[c:23]1[cH:24][c:25]([C:26](=[O:27])[OH:28])[cH:29][cH:30][cH:31]1)[c:11]2[NH:12][CH:13]1[CH2:14][CH2:15][O:16][CH2:17][CH2:18]1.[CH2:99]1[O:100][CH2:101][CH2:102][CH2:103]1.[CH:87]([N:88]([CH:89]([CH3:90])[CH3:91])[CH2:92][CH3:93])([CH3:94])[CH3:95].[Cl:96][CH2:97][Cl:98].[NH2:34][CH2:35][c:36]1[cH:37][c:38](-[c:42]2[cH:43][c:44]([CH2:48][N:49]3[CH2:50][CH:51]([CH3:62])[N:52]([C:55](=[O:56])[O:57][C:58]([CH3:59])([CH3:60])[CH3:61])[CH2:53][CH2:54]3)[cH:45][cH:46][cH:47]2)[cH:39][cH:40][cH:41]1.[P-:63]([F:64])([F:65])([F:66])([F:67])([F:68])[F:69].[n:70]1([O:71][C:72]([N:73]([CH3:74])[CH3:75])=[N+:76]([CH3:77])[CH3:78])[c:79]2[cH:80][cH:81][cH:82][cH:83][c:84]2[n:85][n:86]1>>[CH2:1]([CH3:2])[n:3]1[n:4][cH:5][c:6]2[c:7]1[n:8][c:9]([CH2:32][CH3:33])[c:10]([CH2:19][NH:20][C:21](=[O:22])[c:23]1[cH:24][c:25]([C:26](=[O:27])[NH:34][CH2:35][c:36]3[cH:37][c:38](-[c:42]4[cH:43][c:44]([CH2:48][N:49]5[CH2:50][CH:51]([CH3:62])[N:52]([C:55](=[O:56])[O:57][C:58]([CH3:59])([CH3:60])[CH3:61])[CH2:53][CH2:54]5)[cH:45][cH:46][cH:47]4)[cH:39][cH:40][cH:41]3)[cH:29][cH:30][cH:31]1)[c:11]2[NH:12][CH:13]1[CH2:14][CH2:15][O:16][CH2:17][CH2:18]1

Participants

8

Reactant 7

HCID 6344DichloromethaneHCID 8028TetrahydrofuranHCID 9886HexafluorophosphateHCID 81531DiisopropylethylamineHCID 130500O-benzotriazol-1-yl-tetramethyluroniumHCID 578132773-[({[1,6-Diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methyl}amino)carbonyl]benzoic AcidHCID 178430280HCID 178430280, compound

Product 1

HCID 70989682HCID 70989682, compound

Sources & evidence

ORD record
ord-a76fdd5caf9041e991596281c4bbdde4
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

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