Hydrochloric Acid → HCID 68577686, compound

HRID 642716Notes

Reaction equation

Cl.[CH2:2]([O:4][C:5]([C:7]1[N:8]([CH2:24][C:25]2[C:34]3[C:29](=[CH:30][CH:31]=[C:32]([F:35])[CH:33]=3)[CH:28]=[CH:27][CH:26]=2)[C:9]2[C:14]([C:15]=1[CH2:16][N:17](S(C)(=O)=O)C)=[CH:13][C:12]([F:23])=[CH:11][CH:10]=2)=[O:6])[CH3:3]>>[CH2:2]([O:4][C:5]([C:7]1[N:8]([CH2:24][C:25]2[C:34]3[C:29](=[CH:30][CH:31]=[C:32]([F:35])[CH:33]=3)[CH:28]=[CH:27][CH:26]=2)[C:9]2[C:14]([C:15]=1[CH2:16][NH2:17])=[CH:13][C:12]([F:23])=[CH:11][CH:10]=2)=[O:6])[CH3:3]

Participants

Reactant 2

HCID 313Hydrochloric Acid

HCID 68578786HCID 68578786, compound

Product 1

HCID 68577686HCID 68577686, compound

Procedure

salt with HCl (prepared according to Example 104.2.) was converted to 5-fluoro-1-(7-fluoro-naphthalen-1-ylmethyl)-3-[(methanesulfonyl-methyl-amino)-methyl]-1H-indole-2-carboxylic acid ethyl ester as described in Example 77.1. which was hydrolyzed as described in the general procedure B (Exp. 2.2) to give the title compound as a white solid. MS: 457.4 ([M−H]−).

Sources & evidence

ORD record: ord-c72638a7c6f048e6b1aba6a82f11af16
Source dataset: uspto-grants-2010_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07696240B2

Reaction notes

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