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

Chloride → HCID 22316611, compound

HRID 292346
Notes
Print preview

Reaction equation

HRID 292346 reaction equation
[CH2:34]1[O:35][CH2:36][CH2:37][CH2:38]1.[CH3:11][c:12]1[n:13](-[c:27]2[cH:28][cH:29][c:30]([Br:33])[cH:31][cH:32]2)[c:14](-[c:17]2[cH:18][cH:19][c:20]([S:23](=[O:24])(=[O:25])[CH3:26])[cH:21][cH:22]2)[cH:15][cH:16]1.[CH3:6][CH2:7][CH2:8][CH2:9][Li:10].[Cl-:39].[Cl-:41].[Zn+2:40].[cH:1]1[cH:2][s:3][cH:4][n:5]1.[cH:42]1[cH:43][cH:44][c:45]([P:46]([Pd:47]([P:48]([c:49]2[cH:50][cH:51][cH:52][cH:53][cH:54]2)([c:55]2[cH:56][cH:57][cH:58][cH:59][cH:60]2)[c:61]2[cH:62][cH:63][cH:64][cH:65][cH:66]2)([P:67]([c:68]2[cH:69][cH:70][cH:71][cH:72][cH:73]2)([c:74]2[cH:75][cH:76][cH:77][cH:78][cH:79]2)[c:80]2[cH:81][cH:82][cH:83][cH:84][cH:85]2)[P:86]([c:87]2[cH:88][cH:89][cH:90][cH:91][cH:92]2)([c:93]2[cH:94][cH:95][cH:96][cH:97][cH:98]2)[c:99]2[cH:100][cH:101][cH:102][cH:103][cH:104]2)([c:105]2[cH:106][cH:107][cH:108][cH:109][cH:110]2)[c:111]2[cH:112][cH:113][cH:114][cH:115][cH:116]2)[cH:117][cH:118]1>>[cH:1]1[cH:2][s:3][c:4](-[c:30]2[cH:29][cH:28][c:27](-[n:13]3[c:12]([CH3:11])[cH:16][cH:15][c:14]3-[c:17]3[cH:18][cH:19][c:20]([S:23](=[O:24])(=[O:25])[CH3:26])[cH:21][cH:22]3)[cH:32][cH:31]2)[n:5]1
ParticipantsSources & evidenceReaction notes

Participants

8

Reactant 7

HCID 312Chloride2×HCID 8028TetrahydrofuranHCID 9256ThiazoleHCID 32051Zinc(2+)HCID 223168431-(4-Bromophenyl)-2-methyl-5-[4-(methylsulfonyl)phenyl]-1H-pyrroleHCID 178418339Butyllithium
HCID 178420554
HCID 178420554, compound

Product 1

HCID 22316611HCID 22316611, compound

Sources & evidence

ORD record
ord-d039d10eb7644463b25915344ea79fec
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)
DOI
10.1039/C8SC04228D

Reaction notes

Loading…

On this pageParticipantsSources & evidenceReaction notes