HCID 18771775, compound → HCID 57942353, compound

HRID 1898201Notes

Reaction equation

HRID 1898201 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([NH:11][S:12]([C:15]2[CH:20]=[CH:19][C:18]([Cl:21])=[C:17]([C:22]([F:25])([F:24])[F:23])[CH:16]=2)(=[O:14])=[O:13])[C:5]([C:8](Cl)=[O:9])=[N:6][CH:7]=1.C(OC(=O)[NH:32][C:33]1[CH:38]=[CH:37][CH:36]=[C:35]([NH:39][CH2:40][CH3:41])[N:34]=1)(C)(C)C>>[NH2:32][C:33]1[N:34]=[C:35]([N:39]([CH2:40][CH3:41])[C:8]([C:5]2[C:4]([NH:11][S:12]([C:15]3[CH:20]=[CH:19][C:18]([Cl:21])=[C:17]([C:22]([F:24])([F:23])[F:25])[CH:16]=3)(=[O:13])=[O:14])=[CH:3][C:2]([Cl:1])=[CH:7][N:6]=2)=[O:9])[CH:36]=[CH:37][CH:38]=1

Participants

3

Reactant 2

HCID 18771775HCID 18771775, compoundHCID 57942297HCID 57942297, compound

Product 1

HCID 57942353HCID 57942353, compound

Procedure

The title compound was prepared by procedure analogous to that described in example 325, step 2 using 5-chloro-3-(4-chloro-3-trifluoromethyl-benzenesulfonylamino)-pyridine-2-carbonyl chloride and (6-ethylamino-pyridin-2-yl)-carbamic acid tert-butyl ester.

Sources & evidence

ORD record
ord-9d37c6768e044b6d871b59755107c608
Source dataset
uspto-grants-2013_08
Patent number
US08519135B2

Reaction notes

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