Water → tert-butyl (3R)-3-[(3-chloro-2-pyridinyl)-(4-pyrazolo[1,5-a]pyrimidin-3-ylbenzoyl)amino]piperidine-1-carboxylate

HRID 2015681Notes

Reaction equation

HRID 2015681 reaction equation
O.[cH:1]1[cH:9][n:8]([c:4]2[n:3][cH:2]1)[n:7][cH:6][cH:5]2.[CH3:10][C:11]([O:14][C:15]([N:17]1[CH2:22][C@H:21]([N:23]([c:32]2[c:37]([Cl:38])[cH:36][cH:35][cH:34][n:33]2)[C:24]([c:26]3[cH:31][cH:30][c:29](Br)[cH:28][cH:27]3)=[O:25])[CH2:20][CH2:19][CH2:18]1)=[O:16])([CH3:13])[CH3:12]>>[CH3:10][C:11]([O:14][C:15]([N:17]1[CH2:22][C@H:21]([N:23]([c:32]2[c:37]([Cl:38])[cH:36][cH:35][cH:34][n:33]2)[C:24]([c:26]3[cH:31][cH:30][c:29]([c:5]4[c:4]([n:8]5[n:7][cH:6]4)[n:3][cH:2][cH:1][cH:9]5)[cH:28][cH:27]3)=[O:25])[CH2:20][CH2:19][CH2:18]1)=[O:16])([CH3:13])[CH3:12]

Participants

8

Reactant 3

HCID 962WaterHCID 11636795Pyrazolo(1,5-a)pyrimidineHCID 117652956(R)-tert-butyl 3-(4-bromo-N-(3-chloropyridin-2-yl)benzamido)piperidine-1-carboxylate

Product 1

HCID 118898588tert-butyl (3R)-3-[(3-chloro-2-pyridinyl)-(4-pyrazolo[1,5-a]pyrimidin-3-ylbenzoyl)amino]piperidine-1-carboxylate

Reagents, catalysts & solvents 4

HCID 517044Potassium AcetateReagentHCID 178492617HCID 178492617, compoundCatalystHCID 64052-Methyl-2-butanolSolventHCID 117669-PhenylanthraceneInternal standard

Conditions

Temperature
90 °C

Sources & evidence

ORD record
ord-723411b8d89148d1acd2e8022ca497d6
Source dataset
39k HTE dataset from Pfizer
Original link
View source

Reaction notes

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