HCID 59323011, compound → HCID 59322922, compound

HRID 331234Notes

Reaction equation

HRID 331234 reaction equation
O1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]3[CH:11]([N:14]4[CH2:19][CH2:18][CH:17]([N:20]5[C:24]6[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=6[NH:22][C:21]5=[O:29])[CH2:16][CH2:15]4)[CH2:12][CH2:13][CH:4]([C:5]=23)[CH2:3][CH2:2]1.C1C2=C3C(=CC=C2)C(N)CCC3C1>>[CH2:2]1[C:10]2=[C:5]3[C:6](=[CH:7][CH:8]=[CH:9]2)[CH:11]([N:14]2[CH2:19][CH2:18][CH:17]([N:20]4[C:24]5[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=5[NH:22][C:21]4=[O:29])[CH2:16][CH2:15]2)[CH2:12][CH2:13][CH:4]3[CH2:3]1

Participants

3

Reactant 2

HCID 59323011HCID 59323011, compoundHCID 68702522HCID 68702522, compound

Product 1

HCID 59322922HCID 59322922, compound

Procedure

In the same manner as Example 75(2) and (3) and using 1,2,2a,3,4,5-hexahydroacenaphthylen-5-ylamine, the title compound was obtained as a white solid.

Sources & evidence

ORD record
ord-62e57b74e03c421c9d761f13dba53c15
Source dataset
uspto-grants-2014_11
Patent number
US08877779B2

Reaction notes

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