Tetrahydrofuran → HCID 59369749, compound

HRID 1807326Notes

Reaction equation

[Cl:1][C:2]1[C:3]([F:44])=[C:4]([C@@H:8]2[C@:12]([C:15]3[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:16]=3[F:22])([C:13]#[N:14])[C@H:11]([CH2:23][C:24]([CH3:27])([CH3:26])[CH3:25])[NH:10][C@H:9]2[C:28]([NH:30][C:31]2[C:40]([O:41][CH3:42])=[CH:39][C:34]([C:35]([O:37]C)=[O:36])=[C:33]([F:43])[CH:32]=2)=[O:29])[CH:5]=[CH:6][CH:7]=1.C1COCC1.[OH-].[Na+]>CO>[Cl:21][C:18]1[CH:19]=[CH:20][C:15]([C@@:12]2([C:13]#[N:14])[C@H:11]([CH2:23][C:24]([CH3:26])([CH3:25])[CH3:27])[NH:10][C@@H:9]([C:28]([NH:30][C:31]3[C:40]([O:41][CH3:42])=[CH:39][C:34]([C:35]([OH:37])=[O:36])=[C:33]([F:43])[CH:32]=3)=[O:29])[C@@H:8]2[C:4]2[CH:5]=[CH:6][CH:7]=[C:2]([Cl:1])[C:3]=2[F:44])=[C:16]([F:22])[CH:17]=1

Participants

Conditions

Temperature: 40 °C

Procedure

In a 25 mL round-bottomed flask, methyl 4-((2R,3S,4R,5S)-3-(3-chloro-2-fluorophenyl)-4-(4-chloro-2-fluorophenyl)-4-cyano-5-neopentylpyrrolidine-2-carboxamido)-2-fluoro-5-methoxybenzoate (80 mg, 123 μmol, Eq: 1.00) was combined with THF (2 ml) and MeOH (4 ml) at 45° C. to give a colorless solution. 1 N NaOH (0.5 ml, 1.00 mmol, Eq: 8.11) was added. The reaction mixture was stirred at 40° C. for 2 hr.

Workup

customto give a colorless solution

Sources & evidence

ORD record: ord-afaa248c9add47949a38775f456706c4
Source dataset: uspto-grants-2013_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08354444B2

Reaction notes

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