Ammonium → tert-butyl N-[7-bromo-2-methylthiopyrazolo[1,5-a]pyridin-3-yl]carbamate

HRID 2152830

Reaction equation

HRID 2152830 reaction equation
[Br:25][C:26]([Cl:27])([Cl:28])[C:29]([Br:30])([Cl:31])[Cl:32].[CH2:20]([Li:21])[CH2:22][CH2:23][CH3:24].[CH3:1][S:2][c:3]1[n:4][n:5]2[c:6]([cH:7][cH:8][cH:9][cH:10]2)[c:11]1[NH:12][C:13]([O:14][C:15]([CH3:16])([CH3:17])[CH3:18])=[O:19].[CH3:40][CH2:41][CH2:42][CH2:43][CH2:44][CH3:45].[Cl-:33].[NH4+:34].[O:35]1[CH2:36][CH2:37][CH2:38][CH2:39]1>>[CH3:1][S:2][c:3]1[n:4][n:5]2[c:6]([cH:7][cH:8][cH:9][c:10]2[Br:25])[c:11]1[NH:12][C:13]([O:14][C:15]([CH3:16])([CH3:17])[CH3:18])=[O:19]

Participants

8

Reactant 7

HCID 223AmmoniumHCID 312ChlorideHCID 8028TetrahydrofuranHCID 8058HexaneHCID 694261,2-Dibromo-1,1,2,2-tetrachloroethaneHCID 21984591tert-butyl N-[2-methylthiopyrazolo[1,5-a]pyridin-3-yl]carbamateHCID 178418339Butyllithium

Product 1

HCID 21984585tert-butyl N-[7-bromo-2-methylthiopyrazolo[1,5-a]pyridin-3-yl]carbamate

Sources & evidence

ORD record
ord-7465a19d9c5647bf8ec3657f957622bd
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Linked notes

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