Hydrochloric Acid → N-(Tetrahydro-2H-pyran-2-yloxy) 2-{6-[(naphthalene-2-sulfonyl)-(2-pyrrolidin-1-ylethyl)amino]-3-azabicyclo[3.1.0]hex-3-yl}pyrimidine-5-carboxamide
Reaction equation
[CH3:51][CH2:52][CH2:53][CH2:54][CH2:55][CH2:56][CH3:57].[Cl:40][CH2:41][CH2:42][N:43]1[CH2:44][CH2:45][CH2:46][CH2:47]1.[Cl:48][CH2:49][Cl:50].[ClH:39].[H-:2].[Na+:1].[O:58]=[CH:59][N:60]([CH3:61])[CH3:62].[cH:3]1[c:4]([S:13](=[O:14])(=[O:15])[NH:16][CH:17]2[CH:18]3[CH2:19][N:20]([c:23]4[n:24][cH:25][c:26]([C:29](=[O:30])[NH:31][O:32][CH:33]5[O:34][CH2:35][CH2:36][CH2:37][CH2:38]5)[cH:27][n:28]4)[CH2:21][CH:22]23)[cH:5][cH:6][c:7]2[cH:8][cH:9][cH:10][cH:11][c:12]12>>[cH:3]1[c:4]([S:13](=[O:14])(=[O:15])[N:16]([CH:17]2[CH:18]3[CH2:19][N:20]([c:23]4[n:24][cH:25][c:26]([C:29](=[O:30])[NH:31][O:32][CH:33]5[O:34][CH2:35][CH2:36][CH2:37][CH2:38]5)[cH:27][n:28]4)[CH2:21][CH:22]23)[CH2:41][CH2:42][N:43]2[CH2:44][CH2:45][CH2:46][CH2:47]2)[cH:5][cH:6][c:7]2[cH:8][cH:9][cH:10][cH:11][c:12]12Participants
9
Reactant 8
Product 1
Sources & evidence
- ORD record
- ord-ae71764de4984e43a86f696397df91bc
- Source dataset
- Test data from https://doi.org/10.1039/C8SC04228D
Reaction notes
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