Pyrrolidine → HCID 178504241, compound

Reaction equation

[C:1](#[N:2])[CH:3]1[CH2:4][N:5]([C:7]([CH:8]([CH:9]2[CH2:10][CH2:11]2)[NH:12][C:13](=[O:14])[c:15]2[cH:16][n:17]([CH2:34][O:35][CH2:36][CH2:37][Si:38]([CH3:39])([CH3:40])[CH3:41])[c:18]3[n:19][cH:20][c:21](-[c:24]4[cH:25][c:26]5[n:27][cH:28][cH:29][c:30]([Cl:33])[c:31]5[s:32]4)[n:22][c:23]23)=[O:42])[CH2:6]1.[CH2:43]1[CH2:44][CH2:45][NH:46][CH2:47]1>>[C:1](#[N:2])[CH:3]1[CH2:4][N:5]([C:7]([CH:8]([CH:9]2[CH2:10][CH2:11]2)[NH:12][C:13](=[O:14])[c:15]2[cH:16][n:17]([CH2:34][O:35][CH2:36][CH2:37][Si:38]([CH3:39])([CH3:40])[CH3:41])[c:18]3[n:19][cH:20][c:21](-[c:24]4[cH:25][c:26]5[n:27][cH:28][cH:29][c:30]([N:46]6[CH2:45][CH2:44][CH2:43][CH2:47]6)[c:31]5[s:32]4)[n:22][c:23]23)=[O:42])[CH2:6]1

Participants

Reactant 2

HCID 31268Pyrrolidine

HCID 1785042402-(7-chlorothieno[3,2-b]pyridin-2-yl)-N-[2-(3-cyanoazetidin-1-yl)-1-cyclopropyl-2-oxoethyl]-5-(2-trimethylsilylethoxymethyl)pyrrolo[2,3-b]pyrazine-7-carboxamide

Product 1

HCID 178504241HCID 178504241, compound

Sources & evidence

ORD record: ord-6f7710856e054c5badd0ea7367768a8b
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (5/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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