2-Chloropyrimidine → HCID 10173701, compound

HRID 491447Notes

Reaction equation

HRID 491447 reaction equation
Cl[C:2]1[N:7]=[CH:6][CH:5]=[CH:4][N:3]=1.[CH3:8][O:9][C:10]1[CH:11]=[C:12]([C:18]2[C@@H:27]3[C@@H:22]([CH2:23][CH:24]=[CH:25][CH2:26]3)[C:21](=[O:28])[N:20]([CH:29]3[CH2:34][CH2:33][N:32](C4C=CC([N+]([O-])=O)=CC=4)[CH2:31][CH2:30]3)[N:19]=2)[CH:13]=[CH:14][C:15]=1[O:16][CH3:17]>>[CH3:8][O:9][C:10]1[CH:11]=[C:12]([C:18]2[C@@H:27]3[C@@H:22]([CH2:23][CH:24]=[CH:25][CH2:26]3)[C:21](=[O:28])[N:20]([CH:29]3[CH2:34][CH2:33][N:32]([C:2]4[N:7]=[CH:6][CH:5]=[CH:4][N:3]=4)[CH2:31][CH2:30]3)[N:19]=2)[CH:13]=[CH:14][C:15]=1[O:16][CH3:17]

Participants

3

Procedure

Prepared from 2-Chloro-pyrimidine and starting compound A1 as described for compound 11. Crystallisation from methanol. M.p. 163-166° C.

Workup

  1. customCrystallisation from methanol

Sources & evidence

ORD record
ord-87cc48b8d816415d96eda13dcee693ed
Source dataset
uspto-grants-2009_05
Patent number
US07531540B2

Reaction notes

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