Hydrochloric Acid → 2-[(3R)-3-carbamoyloxypyrrolidin-1-yl]-2-iminoethylmercaptan hydrochloride
反応式
P(=[S:5])([O-])([O-])[O-].[Na+].[Na+].[Na+].Cl.[C:10]([O:13][C@@H:14]1[CH2:18][CH2:17][N:16]([C:19](=[NH:22])[CH2:20][Cl:21])[CH2:15]1)(=[O:12])[NH2:11].Cl>O>[ClH:21].[C:10]([O:13][C@@H:14]1[CH2:18][CH2:17][N:16]([C:19](=[NH:22])[CH2:20][SH:5])[CH2:15]1)(=[O:12])[NH2:11]参加物
実験手順
0.945 g of trisodium phosphorothioate were added to a solution of 1.21 g of 2-[(3R)-3-carbamoyloxypyrrolidin-1-yl]-2-iminoethylchloride hydrochloride in 8 ml of water, kept cooled in ice-water, and the mixture was stirred for about 3 hours at room temperature. After adding 6 ml of 1N hydrochloric acid, the mixture was heated to 50° C. for 30 minutes, and the solvent was then distilled off under reduced pressure. The concentrate was mixed with 8 ml of methanol, insolubles were filtered off, and the filtrate was concentrated under reduced pressure. The concentrate was crystallized by adding ether, and the crystals were collected by filtration and washed with ether, giving 1.25 g of 2-[(3R)-3-carbamoyloxypyrrolidin-1-yl]-2-iminoethylmercaptan hydrochloride.
後処理
- temperaturethe mixture was heated to 50° C. for 30 minutes
- distillationthe solvent was then distilled off under reduced pressure
- additionThe concentrate was mixed with 8 ml of methanol, insolubles
- filtrationwere filtered off
- concentrationthe filtrate was concentrated under reduced pressure
- customThe concentrate was crystallized
- additionby adding ether
- filtrationthe crystals were collected by filtration
- washwashed with ether
出典と根拠
- ORDレコード
- ord-b5740fd6bed84aeb992dc42e98744157
- 出典データセット
- uspto-grants-1988_09
- 特許番号
- US04771046
反応ノート
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