Phenyl carbamate → HCID 16124142, compound

HRID 1175764Notes

Reaction equation

HRID 1175764 reaction equation
[NH2:1][CH:2]1[C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=2[S:8](=[O:16])(=[O:15])[C:4]2([CH2:7][CH2:6][CH2:5]2)[CH2:3]1.[C:17](=O)([O:19]C1C=CC=CC=1)N.[NH2:27][C:28]1[CH:37]=[CH:36][CH:35]=[C:34]2[C:29]=1[CH:30]=[CH:31][N:32]=[CH:33]2>>[O:15]=[S:8]1(=[O:16])[C:4]2([CH2:5][CH2:6][CH2:7]2)[CH2:3][CH:2]([NH:1][C:17]([NH:27][C:28]2[CH:37]=[CH:36][CH:35]=[C:34]3[C:29]=2[CH:30]=[CH:31][N:32]=[CH:33]3)=[O:19])[C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][C:9]1=2

Participants

4

Reactant 3

HCID 69322Phenyl carbamateHCID 707665-AminoisoquinolineHCID 66745588HCID 66745588, compound

Product 1

HCID 16124142HCID 16124142, compound

Procedure

This compound was prepared in the same manner from above (±) 4-Amino-3,4-dihydro-1,1-dioxo-spiro[2H-1-benzothiopyran-2,1′-cyclobutane] and phenyl carbamate of 5-aminoisoquinoline as in step 1V of example 1.

Sources & evidence

ORD record
ord-fb275dccafd74e608129004c00c08592
Source dataset
uspto-grants-2010_11
Patent number
US07842703B2

Reaction notes

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