Diisopropylethylamine → HCID 57827215, compound

HRID 1842170Notes

Reaction equation

HRID 1842170 reaction equation
C1CN([P+](ON2N=[N:25][C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][C:19]2=3)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F.[NH2:34][C:35]1[CH:36]=[CH:37][C:38]([F:61])=[C:39]([C@:41]23[CH2:49][C@@H:48]([O:50][CH2:51][CH3:52])[CH2:47][C@H:46]2[CH2:45][S:44][C:43]([NH:53][C:54](=[O:60])[O:55][C:56]([CH3:59])([CH3:58])[CH3:57])=[N:42]3)[CH:40]=1.C([N:65]([CH2:69]C)C(C)C)(C)C.C(=O)(O)[O-:72].[Na+]>ClCCl>[C:69]([C:21]1[CH:22]=[CH:23][C:24]([C:19]([NH:34][C:35]2[CH:36]=[CH:37][C:38]([F:61])=[C:39]([C@:41]34[CH2:49][C@@H:48]([O:50][CH2:51][CH3:52])[CH2:47][C@H:46]3[CH2:45][S:44][C:43]([NH:53][C:54](=[O:60])[O:55][C:56]([CH3:57])([CH3:59])[CH3:58])=[N:42]4)[CH:40]=2)=[O:72])=[N:25][CH:20]=1)#[N:65]

Participants

6

Reactant 4

HCID 81531DiisopropylethylamineHCID 516892Sodium BicarbonateHCID 2724699PyBOPHCID 57827362HCID 57827362, compound

Product 1

HCID 57827215HCID 57827215, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

PyBOP (205 mg) was added to a solution of tert-butyl(±)-[(4aR*,6S*,7aS*)-7a-(5-amino-2-fluorophenyl)-6-ethoxy-4,4a,5,6,7,7a-hexahydrocyclopenta[d][1,3]thiazin-2-yl]carbamate (52 mg), the compound of Preparation Example 26-(2) (27.3 mg) and N,N-diisopropylethylamine (0.26 mL) in dichloromethane (5.2 mL). The mixture was stirred at room temperature for one hour. The reaction solution was poured into a saturated sodium bicarbonate solution, followed by extraction with ethyl acetate. The extract was washed with a saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The drying agent was removed by filtration and the filtrate was concentrated under reduced pressure. The crude product was purified by silica gel column chromatography to obtain the title compound (45 mg).

Workup

  1. extractionfollowed by extraction with ethyl acetate
  2. washThe extract was washed with a saturated sodium chloride solution
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customThe drying agent was removed by filtration
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. customThe crude product was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-9e154e1c5a9347bbb3afaacaf2714ff1
Source dataset
uspto-grants-2015_02
Patent number
US08946211B2

Reaction notes

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