Pyridine → HCID 68706378, compound

HRID 667758Notes

Reaction equation

HRID 667758 reaction equation
[C:12]([CH3:13])([CH3:14])([CH3:15])[O:16][C:17](=[O:18])[N:19]1[CH2:20][CH2:21][CH:22]([CH2:25][CH2:26][O:27][c:28]2[n:29][c:30]([C:46]#[N:47])[n:31][c:32]([NH:35][CH2:36][CH:37]3[CH2:38][CH2:39][C:40]4([CH2:41][CH2:42][CH2:43]4)[CH2:44][CH2:45]3)[c:33]2[NH2:34])[CH2:23][CH2:24]1.[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[S:8](=[O:9])(=[O:10])[Cl:11].[CH3:57][N:58]([c:59]1[cH:60][cH:61][n:62][cH:63][cH:64]1)[CH3:65].[CH3:66][CH2:67][O:68][C:69]([CH3:70])=[O:71].[Cl:54][CH2:55][Cl:56].[cH:48]1[cH:49][cH:50][n:51][cH:52][cH:53]1>>[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[S:8](=[O:9])(=[O:10])[NH:34][c:33]1[c:28]([O:27][CH2:26][CH2:25][CH:22]2[CH2:21][CH2:20][N:19]([C:17]([O:16][C:12]([CH3:13])([CH3:14])[CH3:15])=[O:18])[CH2:24][CH2:23]2)[n:29][c:30]([C:46]#[N:47])[n:31][c:32]1[NH:35][CH2:36][CH:37]1[CH2:38][CH2:39][C:40]2([CH2:41][CH2:42][CH2:43]2)[CH2:44][CH2:45]1

Participants

7

Reactant 6

HCID 1049PyridineHCID 6344DichloromethaneHCID 8857Ethyl AcetateHCID 142844-(Dimethylamino)pyridineHCID 74740Phenylmethanesulfonyl chlorideHCID 68708811HCID 68708811, compound

Product 1

HCID 68706378HCID 68706378, compound

Sources & evidence

ORD record
ord-7ca275826d7744779522adae13a77d58
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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