反応 #4150926
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-4658d55b31134988a11cdedb4551ef66表示可能な構造データがありません
CC(C)NCC(COC1=CC=C(C=C1)CCOCC2CC2)O化学中間体
構造・識別子・計算物性は CAS によりデータベース記録と照合済みです。
| 中間体 | 1-[4-[2-(cyclopropylmethoxy)ethyl]phenoxy]-3-(propan-2-ylamino)propan-2-ol |
|---|---|
| IUPAC 名 | — |
| CAS番号 | 63659-18-7 |
| データベース ID | 2369 |
| 分子式 | — |
| 分子量 | — |
製品情報
1-[4-[2-(cyclopropylmethoxy)ethyl]phenoxy]-3-(propan-2-ylamino)propan-2-ol (CAS 63659-18-7) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 2369
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-4658d55b31134988a11cdedb4551ef66反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-8c87aefc610c4938b812e0b52a143452反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-4658d55b31134988a11cdedb4551ef66反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2.25 g of 2-Phenyl-3-isopropyl-5-[[4-[2-(cyclopropyl methoxy)ethyl]phenoxy]methyl]oxazolidine from Example 4 was dissolved in a mixture of 10 mLs isopropanol, 10 mLs 5% aqueous hydrochloric acid. It was stirred at room temperature for 16 hrs. The isopropanol was removed under reduced pressure and 30 mLs 1% hydrochloric acid was added. The aqueous phase was washed with 15 mLs of toluene then basified and extracted twice with 10 mL portions of toluene. After removal of the solvent under reduced pressure 1.3 g of white solid was obtained (74% crude yield of betaxolol base). Betaxolol base was converted into its hydrochloride salt by dissolution in toluene and treatment with 1 equivalent of hydrochloric acid in isopropanol. Upon removal of isopropanol under reduced pressure and cooling of the toluene solution the hydrochloride salt of betaxolol was obtained. This solid is recrystallized twice from acetone, 4 mL/g, the second time with charcoal treatment to give a white crystalline solid with a melting point of 111.5°-112.5° C. The isopropanol was removed under reduced pressure and 30 mLs 1% hydrochloric acid was added The aqueous phase was washed with 15 mLs of toluene extracted twice with 10 mL portions of toluene After removal of the solvent under reduced pressure 1.3 g of white solid
ソース ID: ord-abac4399f6194e2388098376917edde2反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2.25 g of 2-Phenyl-3-isopropyl-5-[[4-[2-(cyclopropyl methoxy)ethyl]phenoxy]methyl]oxazolidine from Example 4 was dissolved in a mixture of 10 mLs isopropanol, 10 mLs 5% aqueous hydrochloric acid. It was stirred at room temperature for 16 hrs. The isopropanol was removed under reduced pressure and 30 mLs 1% hydrochloric acid was added. The aqueous phase was washed with 15 mLs of toluene then basified and extracted twice with 10 mL portions of toluene. After removal of the solvent under reduced pressure 1.3 g of white solid was obtained (74% crude yield of betaxolol base). Betaxolol base was converted into its hydrochloride salt by dissolution in toluene and treatment with 1 equivalent of hydrochloric acid in isopropanol. Upon removal of isopropanol under reduced pressure and cooling of the toluene solution the hydrochloride salt of betaxolol was obtained. This solid is recrystallized twice from acetone, 4 mL/g, the second time with charcoal treatment to give a white crystalline solid with a melting point of 111.5°-112.5° C. The isopropanol was removed under reduced pressure and 30 mLs 1% hydrochloric acid was added The aqueous phase was washed with 15 mLs of toluene extracted twice with 10 mL portions of toluene After removal of the solvent under reduced pressure 1.3 g of white solid
ソース ID: ord-abac4399f6194e2388098376917edde2反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: reacting 1-{4-[2-(Cyclopropylmethoxy)ethyl]phenoxy}-2,3-epoxypropane with isopropylamine to produce Betaxolol; and
ソース ID: ord-68c25eceade145838696ca87a1c247b2反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: reacting 1-{4-[2-(Cyclopropylmethoxy)ethyl]phenoxy}-2,3-epoxypropane with isopropylamine to produce Betaxolol.
ソース ID: ord-ba91dbc28c63462ca93bd46a2b37e7f2反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-8c87aefc610c4938b812e0b52a143452反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: reacting 1-{4-[2-(Cyclopropylmethoxy)ethyl]phenoxy}-2,3-epoxypropane with isopropylamine to produce Betaxolol; and
ソース ID: ord-68c25eceade145838696ca87a1c247b2反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: reacting 1-{4-[2-(Cyclopropylmethoxy)ethyl]phenoxy}-2,3-epoxypropane with isopropylamine to produce Betaxolol.
ソース ID: ord-ba91dbc28c63462ca93bd46a2b37e7f2反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: reacting 1-{4-[2-(Cyclopropylmethoxy)ethyl]phenoxy}-2,3-epoxypropane with isopropylamine to produce Betaxolol; and
ソース ID: ord-68c25eceade145838696ca87a1c247b2反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: reacting 1-{4-[2-(Cyclopropylmethoxy)ethyl]phenoxy}-2,3-epoxypropane with isopropylamine to produce Betaxolol.
ソース ID: ord-ba91dbc28c63462ca93bd46a2b37e7f2PubChem References
化合物の公開データベース記録に掲載された情報源です。
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