tert-butyl N-[(3S)-piperidin-3-yl]carbamate → HCID 58386781, compound

HRID 408469

Reaction equation

HRID 408469 reaction equation
[NH:1]1[CH2:6][CH2:5][CH2:4][C@H:3]([NH:7][C:8](=[O:14])[O:9][C:10]([CH3:13])([CH3:12])[CH3:11])[CH2:2]1.Cl[C:16]1[N:21]=[C:20](N2CCCCC2)[C:19]([N+:28]([O-])=O)=[CH:18][N:17]=1>>[NH2:28][C:19]1[C:18]([N:1]2[CH2:6][CH2:5][CH2:4][C@H:3]([NH:7][C:8](=[O:14])[O:9][C:10]([CH3:11])([CH3:13])[CH3:12])[CH2:2]2)=[N:17][CH:16]=[N:21][CH:20]=1

Participants

3

Reactant 2

HCID 1514171tert-butyl N-[(3S)-piperidin-3-yl]carbamateHCID 71472572-Chloro-5-nitro-4-(piperidin-1-yl)pyrimidine

Product 1

HCID 58386781HCID 58386781, compound

Procedure

Method 1 was followed using (S)-tert-butyl piperidin-3-ylcarbamate and 2-chloro-5-nitro-4-(piperidin-1-yl)pyrimidine. LCMS (m/z): 294.2 (MH+), Rt=0.56 min.

Sources & evidence

ORD record
ord-ceebac8809934efb809daf6f6f9825eb
Source dataset
uspto-grants-2014_06
Patent number
US08759338B2

Linked notes

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