Cyclohexyl isocyanate → HCID 178507145, compound

HRID 32480

Reaction equation

HRID 32480 reaction equation
[CH:1]1([N:7]=[C:8]=[O:9])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[N-]=C=O.[NH2:13][C:14]1[N:19]([C:20]2[CH:25]=[CH:24][CH:23]=[C:22]([NH2:26])[CH:21]=2)[CH2:18][N:17]=[C:16]2[O:27][CH:28]=[CH:29][C:15]=12>>[NH2:13][C:14]1[N:19]([C:20]2[CH:25]=[CH:24][CH:23]=[C:22]([NH:26][C:8]([NH:7][CH:1]3[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]3)=[O:9])[CH:21]=2)[CH2:18][N:17]=[C:16]2[O:27][CH:28]=[CH:29][C:15]=12

Participants

4

Reactant 3

HCID 18502Cyclohexyl isocyanateHCID 105034IsocyanateHCID 178507142HCID 178507142, compound

Product 1

HCID 178507145HCID 178507145, compound

Procedure

The compound was prepared following the procedure described in Example 232(b), using cyclohexyl isocyanate as the isocyanate of choice, and 4-Amino-3-(3-aminophenyl)furo[2,3-d]pyrimidine (10) as the diamine of choice. MS(ES) m/e 352 [M+H]+.

Workup

  1. customThe compound was prepared

Sources & evidence

ORD record
ord-b57bcbbc48ad42beb51c475a615ded38
Source dataset
uspto-grants-2008_09
Patent number
US07427623B2

Linked notes

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