Tert-butyl 4-((2-cyanoadamantan-2-yl)methoxy)-5-cyclopropyl-2-fluorobenzoate → HCID 86703731, compound

HRID 1849844Notes

Reaction equation

HRID 1849844 reaction equation
C(C1(COC2C(C3CC3)=CC(C(OC(C)(C)C)=O)=C(F)C=2)C2CC3CC(CC1C3)C2)#N.[CH:32]1([C:35]2[C:36]([O:49][CH2:50][C:51]3([CH:57]([F:59])[F:58])[CH2:56][CH2:55][CH2:54][CH2:53][CH2:52]3)=[CH:37][C:38]([F:48])=[C:39]([CH:47]=2)[C:40]([O:42]C(C)(C)C)=[O:41])[CH2:34][CH2:33]1>>[CH:32]1([C:35]2[C:36]([O:49][CH2:50][C:51]3([CH:57]([F:59])[F:58])[CH2:56][CH2:55][CH2:54][CH2:53][CH2:52]3)=[CH:37][C:38]([F:48])=[C:39]([CH:47]=2)[C:40]([OH:42])=[O:41])[CH2:34][CH2:33]1

Participants

3

Reactant 2

HCID 86703654Tert-butyl 4-((2-cyanoadamantan-2-yl)methoxy)-5-cyclopropyl-2-fluorobenzoateHCID 86703732HCID 86703732, compound

Product 1

HCID 86703731HCID 86703731, compound

Procedure

Following the procedure as described in Example 332 Step 6, and making variations as required to replace tert-butyl 4-((2-cyanoadamantan-2-yl)methoxy)-5-cyclopropyl-2-fluorobenzoate with tert-butyl 5-cyclopropyl-4-((1-(difluoromethyl)-cyclohexyl)methoxy)-2-fluorobenzoate, the title compound was obtained as a beige solid (0.16 g, 96%): MS (ES+) m/z 343.1 (M+1).

Sources & evidence

ORD record
ord-a26f5777f10e48b391ae740a36c10831
Source dataset
uspto-grants-2015_02
Patent number
US08952169B2

Reaction notes

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