HCID 18375676, compound → HCID 69964391, compound

HRID 2300876Notes

Reaction equation

HRID 2300876 reaction equation
[C:1]1([C@@H:7]([NH:9][C:10]2[N:15]=[C:14]([N:16]3[C:20]4[CH:21]=[CH:22][C:23]([Sn](C)(C)C)=[CH:24][C:19]=4[N:18]=[CH:17]3)[CH:13]=[CH:12][N:11]=2)[CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl[C:30]12[N:38]=[CH:37][N:36]=[C:35]1[CH:34]=[N:33][CH:32]=[N:31]2>>[C:1]1([C@@H:7]([NH:9][C:10]2[N:15]=[C:14]([N:16]3[C:20]4[CH:21]=[CH:22][C:23]([C:30]56[N:38]=[CH:37][N:36]=[C:35]5[CH:34]=[N:33][CH:32]=[N:31]6)=[CH:24][C:19]=4[N:18]=[CH:17]3)[CH:13]=[CH:12][N:11]=2)[CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

3

Reactant 2

HCID 18375676HCID 18375676, compoundHCID 69963704HCID 69963704, compound

Product 1

HCID 69964391HCID 69964391, compound

Procedure

The title compound was prepared according to the procedure described in EXAMPLE 424, starting from 2-[(S)-1-Phenylethylamino]-4-[5-trimethylstannylbenzimidazol-1-yl]pyrimidine and 4-chloropurine. Mass spectrum (ESI) 443.4 (M+).

Sources & evidence

ORD record
ord-f775a191502648fdba30b7c4f04f769f
Source dataset
uspto-grants-2002_12
Patent number
US06498165B1

Reaction notes

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