Dichloromethane → (1R,2S)-1-amino-N-(cyclopropylsulfonyl)-2-vinylcyclopropanecarboxamide hydrochloride

HRID 734251Notes

Reaction equation

HRID 734251 reaction equation
C(OC([NH:8][C@:9]1([C:14]([NH:16][S:17]([CH:20]2[CH2:22][CH2:21]2)(=[O:19])=[O:18])=[O:15])[CH2:11][C@H:10]1[CH:12]=[CH2:13])=O)(C)(C)C.[Cl:23]CCl>C(O)(C(F)(F)F)=O>[ClH:23].[NH2:8][C@:9]1([C:14]([NH:16][S:17]([CH:20]2[CH2:22][CH2:21]2)(=[O:19])=[O:18])=[O:15])[CH2:11][C@H:10]1[CH:12]=[CH2:13]

Participants

4

Reactant 2

HCID 6344DichloromethaneHCID 45480526Carbamic acid, N-[(1R,2S)-1-[[(cyclopropylsulfonyl)amino]carbonyl]-2-ethenylcyclopropyl]-, 1,1-dimethylethyl ester

Product 1

HCID 23595124(1R,2S)-1-amino-N-(cyclopropylsulfonyl)-2-vinylcyclopropanecarboxamide hydrochloride

Reagents, catalysts & solvents 1

HCID 6422Trifluoroacetic acidSolvent

Procedure

A solution of the product of Step 2 (3.5 g, 10.6 mmol) in dichloromethane (35 mL) and TFA (32 mL) was stirred at room temperature for 1.5 hours. The volatiles were removed in vacuo and the residue suspended in 1N HCl in diethyl ether (20 mL) and concentrated in vacuo. This procedure was repeated once. The resulting mixture was triturated from pentane and filtered to give the title compound as a hygroscopic, off-white solid (2.60 g, 92%). 1H NMR: (DMSO-d6) δ 1.01-1.15 (m, 4H), 1.69-1.73 (m, 1H), 1.99-2.02 (m, 1H), 2.38 (q, J=9 Hz, 1H), 2.92-2.97 (m, 1H), 5.20 (d, J=11 Hz, 1H), 5.33 (d, J=17 Hz, 1H), 5.52-5.59 (m, 1H), 9.17 (br s, 3H); MS m/z 231 (M++H).

Workup

  1. customThe volatiles were removed in vacuo
  2. concentrationconcentrated in vacuo
  3. customThe resulting mixture was triturated from pentane
  4. filtrationfiltered

Sources & evidence

ORD record
ord-b5c6e048b0bd43668327810af410bbe5
Source dataset
uspto-grants-2009_09
Patent number
US07592336B2

Reaction notes

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