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Pyridine → 2-Acetyl-5-phenylsulphonamido-1,2,3,4-tetrahydroisoquinoline

HRID 88041
Notes
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Reaction equation

HRID 88041 reaction equation
[C:1]([CH3:2])(=[O:3])[N:4]1[CH2:5][c:6]2[cH:7][cH:8][cH:9][c:10]([NH2:14])[c:11]2[CH2:12][CH2:13]1.[CH3:34][CH:35]([OH:36])[CH3:37].[Cl:21][CH2:22][Cl:23].[c:24]1([S:30](=[O:31])(=[O:32])[Cl:33])[cH:25][cH:26][cH:27][cH:28][cH:29]1.[cH:15]1[cH:16][cH:17][n:18][cH:19][cH:20]1>>[C:1]([CH3:2])(=[O:3])[N:4]1[CH2:5][c:6]2[cH:7][cH:8][cH:9][c:10]([NH:14][S:30]([c:24]3[cH:25][cH:26][cH:27][cH:28][cH:29]3)(=[O:31])=[O:32])[c:11]2[CH2:12][CH2:13]1
ParticipantsSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 1049PyridineHCID 3776IsopropanolHCID 6344DichloromethaneHCID 7369Benzenesulfonyl chlorideHCID 212717261-(5-amino-3,4-dihydroisoquinolin-2(1H)-yl)ethanone

Product 1

HCID 212717242-Acetyl-5-phenylsulphonamido-1,2,3,4-tetrahydroisoquinoline

Sources & evidence

ORD record
ord-dcf1f12d6866447ca9cc53e112247a00
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes