2-(Trifluoromethoxy)benzene-1-sulfonyl chloride → HCID 86636244, compound

HRID 541722Notes

Reaction equation

HRID 541722 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].FC(F)(F)C(O)=O.[Cl:22][C:23]1[CH:24]=[N:25][C:26]2[NH:27][C:28]3[CH:29]=[N:30][CH:31]=[C:32]([CH:54]=3)[CH2:33][CH2:34][C:35]3[CH:43]=[C:39]([NH:40][C:41]=1[N:42]=2)[CH:38]=[CH:37][C:36]=3[NH:44][C:45](=[O:53])[CH2:46][CH:47]1[CH2:52][CH2:51][NH:50][CH2:49][CH2:48]1.[F:55][C:56]([F:69])([F:68])[O:57][C:58]1[CH:63]=[CH:62][CH:61]=[CH:60][C:59]=1[S:64](Cl)(=[O:66])=[O:65]>>[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:22][C:23]1[CH:24]=[N:25][C:26]2[NH:27][C:28]3[CH:29]=[N:30][CH:31]=[C:32]([CH:54]=3)[CH2:33][CH2:34][C:35]3[CH:43]=[C:39]([NH:40][C:41]=1[N:42]=2)[CH:38]=[CH:37][C:36]=3[NH:44][C:45](=[O:53])[CH2:46][CH:47]1[CH2:52][CH2:51][N:50]([S:64]([C:59]2[CH:60]=[CH:61][CH:62]=[CH:63][C:58]=2[O:57][C:56]([F:55])([F:68])[F:69])(=[O:66])=[O:65])[CH2:49][CH2:48]1

Participants

3

Reactant 2

HCID 27772152-(Trifluoromethoxy)benzene-1-sulfonyl chlorideHCID 86636131N-[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 tris(trifluoroacetate)

Product 1

HCID 86636244HCID 86636244, compoundYield 16%

Procedure

The desired compound was prepared according to the procedure of Example A42 using 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 tris(trifluoroacetate) and 2-(trifluoromethoxy)benzenesulfonyl chloride as starting materials in 16% yield. LCMS for C31H30ClF3N7O4S (M+H)+: m/z=688.2.

Sources & evidence

ORD record
ord-f5fb3304ffd44f0991d24a53bec546ae
Source dataset
uspto-grants-2014_10
Patent number
US08871753B2

Reaction notes

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