2-Chloro-6-nitroquinoline → HCID 68633135, compound

HRID 1928714Notes

Reaction equation

HRID 1928714 reaction equation
Cl[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N+:12]([O-:14])=[O:13])[CH:8]=2)[N:3]=1.[O:15]1[C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=2[CH:17]([NH2:24])[CH2:16]1>>[O:15]1[C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=2[CH:17]([NH:24][C:2]2[CH:11]=[CH:10][C:9]3[C:4](=[CH:5][CH:6]=[C:7]([N+:12]([O-:14])=[O:13])[CH:8]=3)[N:3]=2)[CH2:16]1

Participants

3

Reactant 2

HCID 109217232-Chloro-6-nitroquinolineHCID 137781522,3-Dihydro-1-benzofuran-3-amine

Product 1

HCID 68633135HCID 68633135, compound

Procedure

(2,3-Dihydro-benzofuran-3-yl)-(6-nitro-quinolin-2-yl)-amine was prepared according to step A in general example 2 from 2-chloro-6-nitro-quinoline and 2,3-dihydro-benzofuran-3-ylamine (CAS no.: 109926-23-4); MS: m/e=308.3 (M+H+).

Sources & evidence

ORD record
ord-17393771242e4621bfed5e6dc4327b0a
Source dataset
uspto-grants-2012_05
Patent number
US08183380B2

Reaction notes

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