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Hydrochloric Acid → Ditert-butyl 4-[[4-[(2-methylquinolin-4-yl)methoxy]phenyl]sulfonylamino]pyrrolidine-1,3-dicarboxylate

HRID 2138399
Notes
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Reaction equation

HRID 2138399 reaction equation
[CH3:31][c:32]1[n:33][c:34]2[cH:35][cH:36][cH:37][cH:38][c:39]2[c:40]([CH2:42][O:43][c:44]2[cH:45][cH:46][c:47]([S:50](=[O:51])(=[O:52])[Cl:53])[cH:48][cH:49]2)[cH:41]1.[CH3:54][N:55]([CH3:56])[CH:57]=[O:58].[CH:21]([N:22]([CH2:23][CH3:24])[CH:25]([CH3:26])[CH3:27])([CH3:28])[CH3:29].[ClH:30].[NH2:1][CH:2]1[CH:3]([C:14](=[O:15])[O:16][C:17]([CH3:18])([CH3:19])[CH3:20])[CH2:4][N:5]([C:7](=[O:8])[O:9][C:10]([CH3:11])([CH3:12])[CH3:13])[CH2:6]1>>[NH:1]([CH:2]1[CH:3]([C:14](=[O:15])[O:16][C:17]([CH3:18])([CH3:19])[CH3:20])[CH2:4][N:5]([C:7](=[O:8])[O:9][C:10]([CH3:11])([CH3:12])[CH3:13])[CH2:6]1)[S:50]([c:47]1[cH:46][cH:45][c:44]([O:43][CH2:42][c:40]2[c:39]3[c:34]([n:33][c:32]([CH3:31])[cH:41]2)[cH:35][cH:36][cH:37][cH:38]3)[cH:49][cH:48]1)(=[O:51])=[O:52]
ParticipantsSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 313Hydrochloric AcidHCID 6228DimethylformamideHCID 81531DiisopropylethylamineHCID 219630384-[(2-Methylquinolin-4-yl)methoxy]benzenesulphonyl chlorideHCID 688172481,3-Di-tert-butyl cis-4-aminopyrrolidine-1,3-dicarboxylate

Product 1

HCID 68818596
Ditert-butyl 4-[[4-[(2-methylquinolin-4-yl)methoxy]phenyl]sulfonylamino]pyrrolidine-1,3-dicarboxylate

Sources & evidence

ORD record
ord-fc51dcdf504f43cea3b267e6eccbd02a
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes