HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

HCID 178493043, compound → HCID 178493044, compound

HRID 121083
Notes
Print preview

Reaction equation

HRID 121083 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]([CH2:35][O:36][CH2:37][CH2:38][Si:39]([CH3:40])([CH3:41])[CH3:42])[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]([O:33][CH3:34])[c:31]5[s:32]4)[n:22][c:23]23)=[O:43])[CH2:6]1.[C:44]([CH:45]1[CH2:46][N:47]([C:48](=[O:49])[CH:50]([NH:51][C:52]([c:53]2[c:54]3[c:55]([n:56][cH:57][c:58](-[c:59]4[s:60][c:61]5[c:62]([n:63][cH:64][cH:65][c:66]5[Cl:67])[cH:68]4)[n:69]3)[n:70]([CH2:71][O:72][CH2:73][CH2:74][Si:75]([CH3:76])([CH3:77])[CH3:78])[cH:79]2)=[O:80])[CH:81]2[CH2:82][CH2:83]2)[CH2:84]1)#[N:85]>>[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][nH:17][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]([O:33][CH3:34])[c:31]5[s:32]4)[n:22][c:23]23)=[O:43])[CH2:6]1
ParticipantsSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 178493043HCID 178493043, compoundHCID 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 178493044HCID 178493044, compound

Sources & evidence

ORD record
ord-091706e9261443f19d40a810ff3ccb39
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI
10.1039/C8SC04228D

Reaction notes

Loading…

On this pageParticipantsSources & evidenceReaction notes