2-Chlorobenzenesulfonyl chloride → HCID 59578087, compound

HRID 2194113Notes

Reaction equation

HRID 2194113 reaction equation
C(O[C:4]([C:6]1([CH2:12][CH2:13]OC)[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1)=[O:5])C.[Cl:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[S:23](Cl)(=[O:25])=[O:24].[N:27]1[CH:32]=[CH:31][CH:30]=[C:29]([O:33][C:34]2[CH:39]=[CH:38][C:37]([NH2:40])=[CH:36][CH:35]=2)[CH:28]=1>>[Cl:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[S:23]([N:9]1[CH2:8][CH2:7][C:6]2([C:4](=[O:5])[N:40]([C:37]3[CH:36]=[CH:35][C:34]([O:33][C:29]4[CH:28]=[N:27][CH:32]=[CH:31][CH:30]=4)=[CH:39][CH:38]=3)[CH2:13][CH2:12]2)[CH2:11][CH2:10]1)(=[O:25])=[O:24]

Participants

4

Reactant 3

HCID 761872-Chlorobenzenesulfonyl chlorideHCID 31596314-(Pyridin-3-Yloxy)AnilineHCID 567539694-(2-Methoxy-ethyl)-piperidine-4-carboxylic acid ethyl ester

Product 1

HCID 59578087HCID 59578087, compound

Procedure

Brown crystalline solid. MS (ESI): 498.2 (MH+). This example was prepared in analogy to example 1 step C) to D) from 4-(2-methoxy-ethyl)-piperidine-4-carboxylic acid ethyl ester (example 1 step B)), 2-chlorobenzenesulfonyl chloride and 4-(pyridin-3-yloxy)-phenylamine (synthesis: Yoneda et al; Yakugaku Zasshi; 77; 1957; 944; Chem. Abstr.; 1958; 2855).

Sources & evidence

ORD record
ord-0d1af55ec60148fc838b55c3e8f10c6d
Source dataset
uspto-grants-2012_12
Patent number
US08329904B2

Reaction notes

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