Hydrogen chloride-ethyl acetate → HCID 178484696, compound

HRID 24831Notes

Reaction equation

C(O[C:6]([N:8]([CH2:10][C:11]([NH:13][CH2:14][C:15]1[CH:20]=[CH:19][C:18]([NH:21]/[C:22](=[C:29]2\[C:30](=[O:41])[NH:31][C:32]3[C:37]\2=[CH:36][C:35]([N+:38]([O-:40])=[O:39])=[CH:34][CH:33]=3)/[C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=[CH:17][CH:16]=1)=[O:12])C)=O)(C)(C)C.C(OCC)(=O)C.[ClH:48]>>[ClH:48].[CH3:6][NH:8][CH2:10][C:11]([NH:13][CH2:14][C:15]1[CH:20]=[CH:19][C:18]([NH:21]/[C:22](=[C:29]2\[C:30](=[O:41])[NH:31][C:32]3[C:37]\2=[CH:36][C:35]([N+:38]([O-:40])=[O:39])=[CH:34][CH:33]=3)/[C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=[CH:17][CH:16]=1)=[O:12]

Participants

Reactant 2

HCID 21866389Hydrogen chloride-ethyl acetate

HCID 178484697HCID 178484697, compound

Product 1

HCID 178484696HCID 178484696, compound

Procedure

Prepared analogously to Example 29a from (Z)-3-{1-[4-(N-tert.butoxycarbonyl-N-methylamino)methylcarbonylaminomethyl-phenylamino]-1-phenyl-methylidene}-5-nitro-2-indolinone and ethyl acetate/hydrogen chloride.

Sources & evidence

ORD record: ord-d9688c957feb46b38f8d9582e842df2c
Source dataset: uspto-grants-2005_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06855710B2

Reaction notes

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