(Diethylamino)sulfur trifluoride → HCID 67076606, compound

HRID 1810837Notes

Reaction equation

HRID 1810837 reaction equation
C[O:2][C:3]([C:5]1([NH:14][C:15](=[O:35])[C:16]2[CH:21]=[CH:20][C:19]([CH:22](O)[CH3:23])=[C:18]([O:25][CH2:26][CH2:27][C:28]3[CH:29]=[C:30]([CH3:34])[CH:31]=[CH:32][CH:33]=3)[CH:17]=2)[CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH2:6]1)=[O:4].C(OC(C1(NC(=O)C2C=CC(C(O)C)=C(OCCC3C=C(C)C=CC=3)C=2)CC2C(=CC=CC=2)C1)=O)C.C(N(S(F)(F)[F:78])CC)C>C(Cl)Cl>[F:78][CH:22]([C:19]1[CH:20]=[CH:21][C:16]([C:15]([NH:14][C:5]2([C:3]([OH:2])=[O:4])[CH2:13][C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[CH2:6]2)=[O:35])=[CH:17][C:18]=1[O:25][CH2:26][CH2:27][C:28]1[CH:29]=[C:30]([CH3:34])[CH:31]=[CH:32][CH:33]=1)[CH3:23]

Participants

5

Reactant 3

HCID 123472(Diethylamino)sulfur trifluorideHCID 67076463HCID 67076463, compoundHCID 67076600HCID 67076600, compound

Product 1

HCID 67076606HCID 67076606, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

The mixture of 2-[4-(1-hydroxy-ethyl)-3-(2-m-tolyl-ethoxy)-benzoylamino]-indane-2-carboxylic acid methyl ester and 2-[4-(1-hydroxy-ethyl)-3-(2-m-tolyl-ethoxy)-benzoylamino]-indane-2-carboxylic acid ethyl ester obtained in example 9 (50 mg) was dissolved in DCM, and diethylaminosulfur trifluoride (33 mg, 0.204 mmol) was added in two portions (second portion after 3.5 h). After complete conversion as detected by HPLC, the mixture was partitioned between EA and a saturated aqueous sodium hydrogencarbonate solution and the aqueous phase extracted with EA. The combined organic extracts were dried over sodium sulfate, filtered and evaporated to dryness. The residue was stirred with a HEP/diethyl ether mixture, filtered, and dried in vacuo. The obtained ester was hydrolyzed in analogy to example 2 to give 12 mg of the title compound.

Workup

  1. customthe mixture was partitioned between EA
  2. extractiona saturated aqueous sodium hydrogencarbonate solution and the aqueous phase extracted with EA
  3. dry with materialThe combined organic extracts were dried over sodium sulfate
  4. filtrationfiltered
  5. customevaporated to dryness
  6. filtrationfiltered
  7. customdried in vacuo

Sources & evidence

ORD record
ord-3d5528e3e1af4f3e984d6e54799b4dfc
Source dataset
uspto-grants-2013_01
Patent number
US08362073B2

Reaction notes

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