6-Chloro-5-ethoxypyrimidin-4-amine → HCID 118290314, compound

HRID 57137Notes

Reaction equation

HRID 57137 reaction equation
[N:1]1([CH2:5][CH2:6][N:7]2[CH:11]=[C:10]([C:12]3[CH:17]=[CH:16][N:15]=[C:14]([CH:18]([CH3:20])[CH3:19])[CH:13]=3)[N:9]=[C:8]2[CH:21]2[CH2:26][CH2:25][NH:24][CH2:23][CH2:22]2)[CH2:4][CH2:3][CH2:2]1.Cl[C:28]1[N:33]=[CH:32][N:31]=[C:30]([NH2:34])[C:29]=1[O:35][CH2:36][CH3:37]>>[N:1]1([CH2:5][CH2:6][N:7]2[CH:11]=[C:10]([C:12]3[CH:17]=[CH:16][N:15]=[C:14]([CH:18]([CH3:20])[CH3:19])[CH:13]=3)[N:9]=[C:8]2[CH:21]2[CH2:22][CH2:23][N:24]([C:28]3[N:33]=[CH:32][N:31]=[C:30]([NH2:34])[C:29]=3[O:35][CH2:36][CH3:37])[CH2:25][CH2:26]2)[CH2:4][CH2:3][CH2:2]1

Participants

3

Reactant 2

HCID 735550476-Chloro-5-ethoxypyrimidin-4-amineHCID 894424674-[1-(2-azetidin-1-yl-ethyl)-2-piperidin-4-yl-1H-imidazol-4-yl]-2-isopropyl-pyridine

Product 1

HCID 118290314HCID 118290314, compound

Procedure

The title compound was prepared according to the procedure described for the preparation of compound “1” by using 4-[1-(2-azetidin-1-yl-ethyl)-2-piperidin-4-yl-1H-imidazol-4-yl]-2-isopropyl-pyridine and 6-chloro-5-ethoxy-pyrimidin-4-ylamine as the starting materials. LC-MS (M+H=491, obsd=491).

Workup

  1. customdescribed for the preparation of compound “1”

Sources & evidence

ORD record
ord-929a2bd8191846e2af86e3c6265e9536
Source dataset
uspto-grants-2016_09
Patent number
US09434714B2

Reaction notes

Loading…