2-Propanol, 1-amino-2-methyl- → HCID 58548230, compound

HRID 2368262Notes

Reaction equation

[NH2:1][CH2:2][C:3]([CH3:6])([OH:5])[CH3:4].C[O:8][C:9]([C:11]1[C:15]([NH:16][C:17]([C:19]2[C:24]([NH:25][C:26]3[CH:27]=[N:28][CH:29]=[N:30][CH:31]=3)=[CH:23][CH:22]=[C:21]([CH:32]3[CH2:34][CH2:33]3)[N:20]=2)=[O:18])=[CH:14][N:13]([CH3:35])[N:12]=1)=O>>[OH:5][C:3]([CH3:6])([CH3:4])[CH2:2][NH:1][C:9]([C:11]1[C:15]([NH:16][C:17]([C:19]2[C:24]([NH:25][C:26]3[CH:27]=[N:28][CH:29]=[N:30][CH:31]=3)=[CH:23][CH:22]=[C:21]([CH:32]3[CH2:34][CH2:33]3)[N:20]=2)=[O:18])=[CH:14][N:13]([CH3:35])[N:12]=1)=[O:8]

Participants

Reactant 2

HCID 951022-Propanol, 1-amino-2-methyl-

HCID 700992004-{[6-Cyclopropyl-3-(pyrimidin-5-ylamino)-pyridine-2-carbonyl]-amino}-1-methyl-1H-pyrazole-3-carboxylic acid methyl ester

Product 1

HCID 58548230HCID 58548230, compoundYield 27%

Procedure

According to the general method described in step 5 of example 27, reaction of 1-amino-2-methyl-propan-2-ol with 4-{[6-cyclopropyl-3-(pyrimidin-5-ylamino)-pyridine-2-carbonyl]-amino}-1-methyl-1H-pyrazole-3-carboxylic acid methyl ester provided the title compound (27%) as amorphous yellow solid.

Sources & evidence

ORD record: ord-6b5507ee4c17496fbc613131fdc9dd96
Source dataset: uspto-grants-2014_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08703768B2

Reaction notes

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