Ammonia → HCID 178508978, compound

HRID 2042831Notes

Reaction equation

HRID 2042831 reaction equation
Cl[C:2]1[C:20]([N+:21]([O-:23])=[O:22])=[CH:19][C:5]([C:6]([NH:8][C@H:9]2[CH2:14][CH2:13][C@H:12]([C:15]([F:18])([F:17])[F:16])[CH2:11][CH2:10]2)=[O:7])=[C:4]([O:24][CH2:25][CH2:26][F:27])[N:3]=1.[NH3:28]>C1COCC1>[F:27][CH2:26][CH2:25][O:24][C:4]1[N:3]=[C:2]([NH2:28])[C:20]([N+:21]([O-:23])=[O:22])=[CH:19][C:5]=1[C:6]([NH:8][C@H:9]1[CH2:14][CH2:13][C@H:12]([C:15]([F:18])([F:17])[F:16])[CH2:11][CH2:10]1)=[O:7]

Participants

4

Procedure

The sub-title compound is prepared from 6-chloro-2-(2-fluoro-ethoxy)-5-nitro-N-(trans-4-trifluoromethyl-cyclohexyl)-nicotinamide (1.30 g, 2.98 mmol) and conc. ammonia (0.90 mL, 14.92 mmol) in THF (30 mL) in analogy with method described in example 3c.

Sources & evidence

ORD record
ord-f03129e5112b4400964db7223ec90149
Source dataset
uspto-grants-2013_11
Patent number
US08586604B2

Reaction notes

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