HCID 68310699, compound → HCID 86718163, compound

HRID 1528033Notes

Reaction equation

[Cl:1][C:2]1[CH:3]=[C:4]([NH:9][C:10]2[C:19]3[C:14](=[CH:15][C:16]([C:32]#[C:33]C4CCOC4)=[C:17]([NH:20][C:21]([CH2:23][P:24](=[O:31])([O:28][CH2:29][CH3:30])[O:25][CH2:26][CH3:27])=[O:22])[CH:18]=3)[N:13]=[CH:12][N:11]=2)[CH:5]=[CH:6][C:7]=1[F:8].ClC1C=C(NC2C3C(=CC(C#C[C@@H:61]4[CH2:65][CH2:64][CH2:63][O:62]4)=C(N)C=3)N=CN=2)C=CC=1F>>[Cl:1][C:2]1[CH:3]=[C:4]([NH:9][C:10]2[C:19]3[C:14](=[CH:15][C:16]([C:32]#[C:33][C@@H:61]4[CH2:65][CH2:64][CH2:63][O:62]4)=[C:17]([NH:20][C:21]([CH2:23][P:24](=[O:31])([O:25][CH2:26][CH3:27])[O:28][CH2:29][CH3:30])=[O:22])[CH:18]=3)[N:13]=[CH:12][N:11]=2)[CH:5]=[CH:6][C:7]=1[F:8]

Participants

Reactant 2

HCID 68310699HCID 68310699, compound

HCID 86718164HCID 86718164, compound

Product 1

HCID 86718163HCID 86718163, compound

Procedure

Compound 2.4 was prepared with the same procedure as the preparation of Compound 1.3, using Compound 2.3 instead of Compound 1.2. MS (ESI) m/z=562 (M+1).

Sources & evidence

ORD record: ord-b6de4e4c0ad34dbd9b0d2496a0f2dad6
Source dataset: uspto-grants-2015_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09090588B2

Reaction notes

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