Sodium Carbonate → HCID 57827644, compound

HRID 1842281Notes

Reaction equation

HRID 1842281 reaction equation
[F:1][C:2]1[C:7](B(O)O)=[CH:6][CH:5]=[CH:4][N:3]=1.C(=O)([O-])[O-].[Na+].[Na+].C(OC([N:24]([C:29]1[S:30][CH2:31][C@@H:32]2[CH2:37][CH2:36][CH2:35][C@:33]2([C:38]2[CH:43]=[C:42]([Cl:44])[CH:41]=[C:40](Br)[CH:39]=2)[N:34]=1)C(OC)=O)=O)(C)(C)C>CN(C=O)C.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[Cl:44][C:42]1[CH:43]=[C:38]([C@:33]23[CH2:35][CH2:36][CH2:37][C@H:32]2[CH2:31][S:30][C:29]([NH2:24])=[N:34]3)[CH:39]=[C:40]([C:7]2[C:2]([F:1])=[N:3][CH:4]=[CH:5][CH:6]=2)[CH:41]=1

Participants

6

Conditions

Temperature
85 °C

Procedure

2-Fluoropyridine-3-boronic acid (55.8 mg), tetrakis(triphenylphosphine)palladium (0) (22.9 mg) and a 1 N sodium carbonate solution (396 μL) were added to a solution of the by-product (±)-N-(t-butoxycarbonyl)-N-(methoxycarbonyl)[(4aR*,7aS*)-7a-(3-bromo-5-chlorophenyl)-4,4a,5,6,7,7a-hexahydrocyclopenta[d][1,3]thiazin-2-yl]amine obtained in Preparation Example 71-(2) (100 mg) in DMF (5 mL). After replacement with nitrogen, the mixture was stirred at 85° C. for three hours. The reaction solution was returned to room temperature, and the solvent was evaporated under reduced pressure. The residue was purified by NH-silica gel column chromatography to obtain a crude product. The crude product was further sequentially purified by NH-pTLC and silica gel column chromatography to obtain the title compound (25.6 mg).

Workup

  1. customwas returned to room temperature
  2. customthe solvent was evaporated under reduced pressure
  3. customThe residue was purified by NH-silica gel column chromatography
  4. customto obtain a crude product
  5. customThe crude product was further sequentially purified by NH-pTLC and silica gel column chromatography

Sources & evidence

ORD record
ord-a2e4bdff37e84580a31c6098469ab2d4
Source dataset
uspto-grants-2015_02
Patent number
US08946210B2

Reaction notes

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