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Sodium Ion → 1-(Phenylsulfonyl)-4-chloro-5-azaindole

HRID 183956
Notes
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Reaction equation

HRID 183956 reaction equation
[CH2:28]([N+:29]([CH2:30][CH2:31][CH2:32][CH3:33])([CH2:34][CH2:35][CH2:36][CH3:37])[CH2:38][CH2:39][CH2:40][CH3:41])[CH2:42][CH2:43][CH3:44].[Cl:13][c:14]1[n:15][cH:16][cH:17][c:18]2[c:19]1[cH:20][cH:21][nH:22]2.[Cl:45][CH2:46][Cl:47].[Na+:12].[OH-:11].[S:23]([O-:24])([OH:25])(=[O:26])=[O:27].[c:1]1([S:7](=[O:8])(=[O:9])[Cl:10])[cH:2][cH:3][cH:4][cH:5][cH:6]1>>[c:1]1([S:7](=[O:8])(=[O:9])[n:22]2[c:18]3[cH:17][cH:16][n:15][c:14]([Cl:13])[c:19]3[cH:20][cH:21]2)[cH:2][cH:3][cH:4][cH:5][cH:6]1
ParticipantsSources & evidenceReaction notes

Participants

8

Reactant 7

HCID 923Sodium IonHCID 961HydroxideHCID 6344DichloromethaneHCID 7369Benzenesulfonyl chlorideHCID 16028TetrabutylammoniumHCID 61778Sulfate, hydrogenHCID 141143844-chloro-1H-pyrrolo[3,2-c]pyridine

Product 1

On this pageParticipantsSources & evidenceReaction notes
HCID 181764061-(Phenylsulfonyl)-4-chloro-5-azaindole

Sources & evidence

ORD record
ord-59faf30a254848aab53d0212260925ac
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)
DOI
10.1039/C8SC04228D

Reaction notes

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