Diisopropylethylamine → HCID 118566637, compound

HRID 1056730Notes

Reaction equation

HRID 1056730 reaction equation
[F:1][C:2]1([F:25])[CH2:7][CH2:6][C:5]([CH2:9][NH:10][C:11]([C:13]2[C:14]3[CH:15]=[CH:16][C:17](Cl)=[N:18][C:19]=3[CH:20]=[CH:21][C:22]=2[Cl:23])=[O:12])(O)[CH2:4][CH2:3]1.CCN(C(C)C)C(C)C.[F:35][CH:36]1[CH2:40][NH:39][CH:38]([CH2:41][OH:42])[CH2:37]1>>[F:1][C:2]1([F:25])[CH2:7][CH2:6][CH:5]([CH2:9][NH:10][C:11]([C:13]2[C:14]3[CH:15]=[CH:16][C:17]([N:39]4[CH2:40][CH:36]([F:35])[CH2:37][CH:38]4[CH2:41][OH:42])=[N:18][C:19]=3[CH:20]=[CH:21][C:22]=2[Cl:23])=[O:12])[CH2:4][CH2:3]1

Participants

4

Reactant 3

HCID 81531DiisopropylethylamineHCID 17859296HCID 17859296, compoundHCID 1185560922,6-Dichloro-quinoline-5-carboxylic acid (4,4-difluoro-1-hydroxy-cyclohexylmethyl)-amide

Product 1

HCID 118566637HCID 118566637, compound

Procedure

The title compound was synthesized according to the procedure described in example 1 using 2,6-dichloro-quinoline-5-carboxylic acid (4,4-difluoro-1-hydroxycyclohexylmethyl)-amide, DIPEA and 4-fluoro-2-hydroxymethyl-pyrrolidine. 1H NMR (400 MHz, DMSO-d6) δ ppm 7.75 (1H), 7.48 (2H), 6.69 (1H), 5.33-5.52 (1H), 4.31 (m, 1H), 3.89 (m, 1H), 3.70 (m, 3H), 3.55 (m, 1H), 3.26 (m, 2H), 2.44 (m, 2H), 2.06 (m, 2H), 1.85 (m, 2H), 1.74-1.76 (m, 5H), 1.27-1.32 (m, 2H). m/z: 456 [M+H]

Sources & evidence

ORD record
ord-b733639f13bf4aa091e15e273ba755aa
Source dataset
uspto-grants-2016_07
Patent number
US09399623B2

Reaction notes

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