3-Cyanobenzoyl chloride → HCID 86636221, compound

HRID 541700Notes

Reaction equation

HRID 541700 reaction equation
[F:1][C:2]([F:7])([F:6])[C:3]([OH:5])=[O:4].[F:8][C:9]([F:14])([F:13])[C:10]([OH:12])=[O:11].[Cl:15][C:16]1[CH:17]=[N:18][C:19]2[NH:20][C:21]3[CH:22]=[N:23][CH:24]=[C:25]([CH:47]=3)[CH2:26][CH2:27][C:28]3[CH:36]=[C:32]([NH:33][C:34]=1[N:35]=2)[CH:31]=[CH:30][C:29]=3[NH:37][C:38](=[O:46])[CH2:39][CH:40]1[CH2:45][CH2:44][NH:43][CH2:42][CH2:41]1.[C:48]([C:50]1[CH:51]=[C:52]([CH:56]=[CH:57][CH:58]=1)[C:53](Cl)=[O:54])#[N:49]>>[F:1][C:2]([F:7])([F:6])[C:3]([OH:5])=[O:4].[F:8][C:9]([F:14])([F:13])[C:10]([OH:12])=[O:11].[Cl:15][C:16]1[CH:17]=[N:18][C:19]2[NH:20][C:21]3[CH:22]=[N:23][CH:24]=[C:25]([CH:47]=3)[CH2:26][CH2:27][C:28]3[CH:36]=[C:32]([NH:33][C:34]=1[N:35]=2)[CH:31]=[CH:30][C:29]=3[NH:37][C:38](=[O:46])[CH2:39][CH:40]1[CH2:45][CH2:44][N:43]([C:53](=[O:54])[C:52]2[CH:56]=[CH:57][CH:58]=[C:50]([C:48]#[N:49])[CH:51]=2)[CH2:42][CH2:41]1

Participants

3

Reactant 2

HCID 3084833-Cyanobenzoyl chlorideHCID 86636208N-[6-chloro-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-12-yl]-2-piperidin-4-ylacetamide bis(trifluoroacetate)

Product 1

HCID 86636221HCID 86636221, compoundYield 14%

Procedure

The desired compound was prepared according to the procedure of Example A20 using of N-[6-chloro-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-12-yl]-2-piperidin-4-ylacetamide bis(trifluoroacetate) and 3-cyanobenzoyl chloride as starting materials in 14% yield. LCMS for C32H30ClN8O2 (M+H)+: m/z=593.2.

Sources & evidence

ORD record
ord-722986ed0f3f4791b108944145c3527b
Source dataset
uspto-grants-2014_10
Patent number
US08871753B2

Reaction notes

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