1-Adamantanecarbonyl chloride → HCID 20437845, compound
Reaction equation
[OH:1][CH2:2][CH2:3][C:4]1[C:5]2[N:6]([N:17]=[CH:18][N:19]=2)[C:7]([NH2:16])=[N:8][C:9]=1[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[C:20]12([C:30](Cl)=[O:31])[CH2:29][CH:24]3[CH2:25][CH:26]([CH2:28][CH:22]([CH2:23]3)[CH2:21]1)[CH2:27]2>>[C:20]12([C:30]([O:1][CH2:2][CH2:3][C:4]3[C:5]4[N:6]([N:17]=[CH:18][N:19]=4)[C:7]([NH2:16])=[N:8][C:9]=3[C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)=[O:31])[CH2:27][CH:26]3[CH2:25][CH:24]([CH2:23][CH:22]([CH2:28]3)[CH2:21]1)[CH2:29]2Participants
3
Procedure
The title compound was prepared by the method of Example 2 using 2.5 g (0.01 mole) of the product compound of Example 1 and 2.0 g (0.01 mole) of 1-adamantanecarbonyl chloride, except that the solution was not divided before purification.
Workup
- customwas not divided before purification
Sources & evidence
- ORD record
- ord-68504e3b067c49c485ab088f8b2b8e01
- Source dataset
- uspto-grants-1984_11
- Patent number
- US04483987
Reaction notes
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